Over-the-counter drug · OTC MONOGRAPH DRUG
Pain Relief (Acetaminophen) NDC 21130-431
Acetaminophen 500 mg/1 · Tablet · Oral · BETTER LIVING BRANDS LLC.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 21130-431-01 | 2113004310121130043101 | 1 BOTTLE in 1 CARTON (21130-431-01) / 100 TABLET in 1 BOTTLEMarketed from Jun 22, 2023 | |
| 21130-431-05 | 2113004310521130043105 | 1 BOTTLE in 1 CARTON (21130-431-05) / 50 TABLET in 1 BOTTLEMarketed from Jun 22, 2023 | |
| 21130-431-15 | 2113004311521130043115 | 150 TABLET in 1 BOTTLE (21130-431-15)Marketed from Jun 1, 2023 | |
| 21130-431-25 | 2113004312521130043125 | 1 BOTTLE in 1 CARTON (21130-431-25) / 250 TABLET in 1 BOTTLEMarketed from Jun 1, 2023 | |
| 21130-431-42 | 2113004314221130043142 | 1 BOTTLE in 1 CARTON (21130-431-42) / 24 TABLET in 1 BOTTLEMarketed from Jun 1, 2023 | |
| 21130-431-50 | 2113004315021130043150 | 500 TABLET in 1 BOTTLE (21130-431-50)Marketed from Jun 1, 2023 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Pain Relief
- Generic name (nonproprietary)
- acetaminophen
- Active ingredients
- Acetaminophen — 500 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- BETTER LIVING BRANDS LLC.NDC labeler code 21130
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication M 013
- Marketing start
- Listing expires
- Identifiers
- Product ID 21130-431_3a0b3c00-eacb-ff6f-e063-6394a90a70d7SPL ID 3a0b3c00-eacb-ff6f-e063-6394a90a70d7SPL set ID f3005d0c-424e-0ab3-e053-2995a90a1c10RxCUI 198440UNII 362O9ITL9D
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N421130043101followed by a unit qualifier and the quantityPackage 21130-0431-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
Uses temporarily relieves minor aches and pains due to: the common cold headache backache minor pain of arthritis toothache muscular aches premenstrual and menstrual cramps temporarily reduces fever
Excerpt only. Read the full label for complete information.
About NDC 21130-431
- What is NDC 21130-431?
- 21130-431 is the product NDC for Pain Relief (acetaminophen), Acetaminophen 500 mg/1 tablet, listed with the FDA by BETTER LIVING BRANDS LLC.. It has 6 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Pain Relief (Acetaminophen).
- What is the active ingredient?
- Acetaminophen.
- Who is the labeler?
- BETTER LIVING BRANDS LLC., NDC labeler code 21130. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Pain Relief?
- 62 other product NDCs are listed under this name. See all Pain Relief NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Pain Relief products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Pain Reliefacetaminophen | Acetaminophen 325 mg/1 | TabletOral | Shield Pharmaceuticals Corp. | 83059-0160 | — |
| Pain Reliefmenthol spray | Menthol 76.6 mg/mL | SprayTopical | Owell Naturals Brand, LLC | 83570-003 | 83570-0003-02 |
| Pain Reliefarnica montana, belladonna, gelsemium sempervirens, gnaphalium polycephalum, magnesia phosphorica, sanguinaria canadensis, salix alba | Arnica montana whole 6 [hp_X]/1 + 6 more ingredients | TabletOral | NaturalCare | 70163-0022 | 70163-0022-01 |
| pain reliefacetaminophen | Acetaminophen 500 mg/1 | Tablet, Film coatedOral | HyVee Inc | 42507-813 | 42507-0813-78 |
| Pain Reliefmenthol | Menthol 10.5 g/100mL | SprayTopical | Trifecta Pharmaceuticals USA, LLC. | 69396-175 | 69396-0175-03 |
| Pain Reliefacetaminophen | Acetaminophen 500 mg/1 | TabletOral | HYVEE INC | 42507-103 | 42507-0103-04 |
| Pain Reliefacetaminophen | Acetaminophen 650 mg/1 | Tablet, Extended releaseOral | HYVEE INC | 42507-303 | 42507-0303-03 |
| Pain Reliefacetaminophen | Acetaminophen 500 mg/1 | Tablet, CoatedOral | HYVEE INC | 42507-404 | 42507-0404-09 |
| Pain Reliefacetaminophen | Acetaminophen 500 mg/1 | Tablet, CoatedOral | HYVEE INC | 42507-592 | 42507-0592-03 |
| Pain Relieflidocaine | Lidocaine .04 g/g | PatchTopical | Shanghai Chuangshi Medical Technology (Group) Co., Ltd. | 73557-189 | 73557-0189-30 |
Other NDCs under M 013
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Childrens Acetaminophenacetaminophen | Acetaminophen 160 mg/5mL | SuspensionOral | Grocery Outlet, Inc. | 85828-922 |
| Pain Relief Regular Strengthacetaminophen | Acetaminophen 325 mg/1 | TabletOral | CHAIN DRUG MARKETING ASSOCIATION INC | 83324-076 |
| equate pain and fever childrensacetaminophen | Acetaminophen 160 mg/5mL | SuspensionOral | Wal-Mart Stores Inc | 49035-042 |
| good neighbor pharmacy childrens pain and feveracetaminophen | Acetaminophen 160 mg/5mL | SuspensionOral | Amerisource Bergen | 46122-210 |
| Aspirin | Aspirin 81 mg/1 | Tablet, Delayed releaseOral | GOODSENSE | 50804-880 |
| Tylenol PM Extra Strengthacetaminophen and diphenhydramine hydrochloride | Acetaminophen 500 mg/1; Diphenhydramine hydrochloride 25 mg/1 | Tablet, Film coatedOral | Morning Star OTC | 53209-1002 |
| Acetaminophen | Acetaminophen 500 mg/1 | TabletOral | Cardinal Health 107, LLC | 55154-7897 |
| Headache Formula Extra Strengthacetaminophen, aspirin, caffeine | Acetaminophen 250 mg/1 + 2 more ingredients | Tablet, Film coatedOral | ARMY AND AIR FORCE EXCHANGE SERVICE | 55301-334 |
| childrens pain and feveracetaminophen | Acetaminophen 160 mg/5mL | SuspensionOral | Walgreen Company | 0363-1239 |
| Tylenol PMacetaminophen, diphenhydramine hydrochloride | Acetaminophen 500 mg/1; Diphenhydramine hydrochloride 25 mg/1 | Tablet, Film coatedOral | Savings Distributors LLC | 73097-013 |
| Alka-Seltzer Originalanhydrous citric acid, aspirin, and sodium bicarbonate | Anhydrous citric acid 1000 mg/1 + 2 more ingredients | Tablet, EffervescentOral | Bayer HealthCare LLC. | 0280-4000 |
| Aspirin Low Doseaspirin | Aspirin 81 mg/1 | Tablet, Delayed releaseOral | Strategic Sourcing Services LLC | 70677-1260 |
| basic care infants pain and feveracetaminophen | Acetaminophen 160 mg/5mL | SuspensionOral | Amazon.com Services LLC | 72288-946 |
| Acetaminophen | Acetaminophen 500 mg/1 | TabletOral | Sportpharm LLC | 85766-223 |
| Pain Relief Aspirin Low Doseaspirin | Aspirin 81 mg/1 | Tablet, Delayed releaseOral | Rite Aid Corporation | 11822-0600 |
| Equaline Effervescent Antacid and Pain Reliefaspirin, citric acid, sodium bicarbonate | Aspirin 325 mg/1 + 2 more ingredients | Tablet, EffervescentOral | United Natural Foods, Inc. dba UNFI | 41163-421 |
| Night Time Severe Cold and Cough Reliefacetaminophen, diphenhydramine hcl, phenylephrine hcl | Acetaminophen 325 mg/15mL + 2 more ingredients | LiquidOral | Chain Drug Consortium, LLC | 68016-154 |
| Tension Headache Relief | Acetaminophen 500 mg/1; Caffeine 65 mg/1 | Capsule, CoatedOral | Allegiant Health | 69168-001 |
| Childrens Acetaminophenacetaminophen | Acetaminophen 160 mg/5mL | SuspensionOral | Proficient Rx LP | 71205-263 |
| Chewable Aspirinaspirin | Aspirin 81 mg/1 | Tablet, ChewableOral | Chain Drug Marketing Association, Inc. | 83324-075 |
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