Over-the-counter drug · OTC MONOGRAPH DRUG
Pain Relief (Analgesic menthol) NDC 47682-321
Menthol 70 mg/L · Spray · Topical · Unifirst First Aid Corporation
NDC codes
FDA NDC DirectoryProduct NDC (as listed)47682-321Labeler and product segments. Claims need a package NDC.
Product NDC at billing width47682-0321Add the package segment from the table below.
| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 47682-321-02 | 4768203210247682032102 | .059 L in 1 BOTTLE, SPRAY (47682-321-02)Marketed from Apr 1, 2019 |
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)
- analgesic menthol
- Active ingredients
- Menthol — 70 mg/L
- Dosage form
- Spray
- Route
- Topical
- Labeler
- Unifirst First Aid CorporationNDC labeler code 47682
- Product type
- Over-the-counter drug
- Marketing category
- OTC monograph drugApplication M 015
- Marketing start
- Listing expires
- Identifiers
- Product ID 47682-321_3e4ee639-9aef-38c5-e063-6394a90a9ad3SPL ID 3e4ee639-9aef-38c5-e063-6394a90a9ad3SPL set ID 8162d22d-04c0-de07-e053-2991aa0a9975UNII L7T10EIP3AUPC 0347682301774
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. Topical products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N447682032102followed by a unit qualifier and the quantityPackage 47682-0321-02. 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 Temporary relief of minor aches and pains of muscles and joints.
Excerpt only. Read the full label for complete information.
About NDC 47682-321
- What is NDC 47682-321?
- 47682-321 is the product NDC for Pain Relief (analgesic menthol), Menthol 70 mg/L spray, listed with the FDA by Unifirst First Aid Corporation. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Pain Relief (Analgesic Menthol).
- What is the active ingredient?
- Menthol.
- Who is the labeler?
- Unifirst First Aid Corporation, NDC labeler code 47682. 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 015
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 |
|---|---|---|---|---|
| Pramoxine Hydrochloride Anorectalpramoxine hydrochloride | Pramoxine hydrochloride 1 mg/mL | LotionTopical | Stratus Pharmaceuticals | 58980-522 |
| Ma Ying Long Musk Hemorrhoidspetrolatum, zinc oxide | Petrolatum 779.9 mg/g; Zinc oxide 76 mg/g | OintmentTopical | Mayinglong Pharmaceutical Group Co., Ltd. | 68511-997 |
| Mayinglong Hemorrhoidalpetrolatum, zinc oxide | Petrolatum 779.9 mg/g; Zinc oxide 76 mg/g | OintmentTopical | Mayinglong Pharmaceutical Group Co., Ltd. | 68511-998 |
| hemorrhoidal maximum strength pain reliefglycerin, phenylephrine hcl, pramoxine hcl, white petrolatum | Glycerin 14.4 g/100g + 3 more ingredients | CreamTopical | Kroger Company | 30142-944 |
| Preparation Hcocoa butter, phenylephrine hydrochloride, and witch hazel | — | Kit | Haleon US Holdings LLC | 0573-2884 |
| Hemorrhoidalmineral oil, petrolatum, phenylephrine hcl | Mineral oil 14 g/100g + 2 more ingredients | OintmentRectal | Kroger Company | 30142-188 |
| rexall hemorrhoidalcocoa butter, phenylephrine hcl | Cocoa butter 2211 mg/1; Phenylephrine hydrochloride 6.5 mg/1 | SuppositoryRectal | Dolgencorp Inc | 55910-279 |
| Witch Hazel | Witch hazel 860 mg/mL | LiquidTopical | CVS Pharmacy, Inc. | 59779-045 |
| Dermatool Hemorrhoidalglycerin, lidocaine, petrolatum, phenylephrine hcl | Lidocaine 5 g/100g + 3 more ingredients | CreamTopical | Papalo Group LLC | 84728-413 |
| Acolye Numbing Cream Anorectal(Hemorrhoidal) Creamlidocaine | Lidocaine 5 g/100g | CreamTopical | Guangzhou Haishi Biological Technology Co., Ltd. | 60771-0028 |
| Hemorrhoid Anestheticmineral oil, petrolatum, phenylephrine hcl | Petrolatum .749 g/g + 2 more ingredients | OintmentTopical | Savvy Care and Cosmetics | 83650-110 |
| hemorrhoidalcocoa butter, phenylephrine hcl | Cocoa butter 2211 mg/1; Phenylephrine hydrochloride 6.5 mg/1 | SuppositoryRectal | Meijer Distribution Inc | 41250-279 |
| Lidocaine Numbing Creamlidocaine | Lidocaine .05 g/g | CreamTopical | Shanghai Chuangshi Medical Technology (Group) Co., Ltd. | 73557-311 |
| RWWXII Deep Numbing Cream(Anorectal Hemorrhoidal Cream)lidocaine | Lidocaine 5 g/100g | CreamTopical | Guangzhou Haishi Biological Technology Co., Ltd. | 60771-0027 |
| Barrier Protectant Creambarrier cream | Menthol 1 mg/g; Zinc oxide 200 mg/g | OintmentTopical | Cardinal Health | 63517-003 |
| ER Hemorrhoidphenylephrine hcl | Mineral oil .14 g/g + 2 more ingredients | CreamRectal | EVER READY FIRST AID | 72976-018 |
| ANIXIKE Numbinglidocaine4% numbing | Lidocaine 4 g/100g | CreamTopical | Jiangxi Yudexi Pharmaceutical Co., LTD | 85248-166 |
| Meijer Maximum strength pain relieving cleansingbenzalkonium chloride and lidocaine hydrochloride | Benzalkonium chloride .13 g/100mL; Lidocaine hydrochloride 4 g/100mL | LiquidTopical | MEIJER DISTRIBUTION, INC. | 41250-287 |
| hemorrhoidalglycerin, phenylephrine hcl, pramoxine hcl, white petrolatum | Glycerin 14.4 g/100g + 3 more ingredients | CreamTopical | Meijer Distribution Inc | 41250-944 |
| Equaline Hemorrhoidalcocoa butter, phenylephrine hcl | Cocoa butter 2211 mg/1; Phenylephrine hydrochloride 6.5 mg/1 | SuppositoryRectal | United Natural Foods, Inc. dba UNFI | 41163-279 |
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