What is NDC 62795-1012?

62795-1012 is the product NDC for Mucus Relief, Antimony potassium tartrate 5 [hp_X]/1 + 8 more ingredients tablet, listed with the FDA by MediNatura Inc. It has 2 package NDCs, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Mucus Relief (ANTIMONY POTASSIUM TARTRATE, ATROPA BELLADONNA, BRYONIA ALBA WHOLE, ANEMONE AMERICANA, HYOSCYAMUS NIGER, IPECAC, LOBELIA INFLATA, HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED, and LOBARIA PULMONARIA).

What is the active ingredient?

Antimony potassium tartrate, Atropa belladonna, Bryonia alba whole, Anemone hepatica var. Obtusa, Hyoscyamus niger, Ipecac, Lobelia inflata, Human sputum, Bordetella pertussis infected, Lobaria pulmonaria.

MediNatura Inc, NDC labeler code 62795. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Mucus Relief?

70 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Mucus Relief NDC 62795-1012 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)62795-1012Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62795-1012Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
62795-1012-2	6279510120262795101202	100 TABLET in 1 BOTTLE (62795-1012-2)Marketed from Dec 14, 2022
62795-1012-3	6279510120362795101203	1 BOTTLE in 1 CARTON (62795-1012-3) / 100 TABLET in 1 BOTTLEMarketed from Jan 1, 2015

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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): Mucus Relief
Generic name (nonproprietary): antimony potassium tartrate, atropa belladonna, bryonia alba whole, anemone americana, hyoscyamus niger, ipecac, lobelia inflata, human sputum, bordetella pertussis infected, and lobaria pulmonaria
Active ingredients: Antimony potassium tartrate — 5 [hp_X]/1Atropa belladonna — 6 [hp_X]/1Bryonia alba whole — 6 [hp_X]/1Anemone hepatica var. Obtusa — 6 [hp_X]/1Hyoscyamus niger — 5 [hp_X]/1Ipecac — 6 [hp_X]/1Lobelia inflata — 4 [hp_X]/1Human sputum, Bordetella pertussis infected — 30 [hp_X]/1Lobaria pulmonaria — 5 [hp_X]/1
Dosage form: Tablet
Route: Oral
Labeler: MediNatura IncNDC labeler code 62795
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 1, 2015
Listing expires: Dec 31, 2026
Identifiers: Product ID 62795-1012_906bf8a5-cca6-4a15-9de3-4f4111da1c2fSPL ID 906bf8a5-cca6-4a15-9de3-4f4111da1c2fSPL set ID 6338dc4f-b2d9-4b9a-a397-0440cbd1345aUNII DL6OZ476V3, WQZ3G9PF0H, 56K0VVT47P, 6ICN6T7FEM, 4WRK2153H3, 62I3C8233L, 9PP1T3TC5U, U364V64HUN, D1YM0P5Z2T

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

N462795101202 followed by a unit qualifier and the quantity

Package 62795-1012-02. 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 Dec 14, 2022.

Indications (excerpt from the label)

Uses: For the temporary relief of minor chest congestion and cough due to mucus build-up

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 62795-1012

What is NDC 62795-1012?: 62795-1012 is the product NDC for Mucus Relief, Antimony potassium tartrate 5 [hp_X]/1 + 8 more ingredients tablet, listed with the FDA by MediNatura Inc. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Mucus Relief (ANTIMONY POTASSIUM TARTRATE, ATROPA BELLADONNA, BRYONIA ALBA WHOLE, ANEMONE AMERICANA, HYOSCYAMUS NIGER, IPECAC, LOBELIA INFLATA, HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED, and LOBARIA PULMONARIA).
What is the active ingredient?: Antimony potassium tartrate, Atropa belladonna, Bryonia alba whole, Anemone hepatica var. Obtusa, Hyoscyamus niger, Ipecac, Lobelia inflata, Human sputum, Bordetella pertussis infected, Lobaria pulmonaria.
Who is the labeler?: MediNatura Inc, NDC labeler code 62795. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Mucus Relief?: 70 other product NDCs are listed under this name. See all Mucus Relief NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Mucus Relief NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Mucus Reliefguaifenesin	Guaifenesin 400 mg/1	TabletOral	Geri-Care Pharmaceuticals, Corp	57896-718	57896-0718-01
Mucus Reliefguaifenesin	Guaifenesin 1200 mg/1	Tablet, Extended releaseOral	YYBA Corp	73581-403	73581-0403-0173581-0403-03
Mucus Reliefguaifenesin	Guaifenesin 600 mg/1	Tablet, Extended releaseOral	Grocery Outlet, Inc.	85828-723	85828-0723-02
mucus reliefguaifenesin	Guaifenesin 1200 mg/1	Tablet, Multilayer, Extended releaseOral	CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED	51316-728	51316-0728-5551316-0728-74
Mucus Reliefguaifenesin	Guaifenesin 600 mg/1	Tablet, Extended releaseOral	HYVEE INC	42507-253	42507-0253-03
Mucus Reliefguaifenesin	Guaifenesin 600 mg/1	Tablet, Extended releaseOral	Pioneer Life Sciences, LLC	72090-011	72090-0011-0172090-0011-02
Mucus Reliefguaifenesin	Guaifenesin 600 mg/1	Tablet, Extended releaseOral	NUVICARE LLC	84324-026	84324-0026-01
Mucus Reliefguaifenesin	Guaifenesin 1200 mg/1	Tablet, Extended releaseOral	Pioneer Life Sciences, LLC	72090-012	72090-0012-0172090-0012-0272090-0012-03
Mucus Reliefguaifenesin	Guaifenesin 1200 mg/1	Tablet, Extended releaseOral	NUVICARE LLC	84324-034	84324-0034-01
Mucus Reliefguaifenesin	Guaifenesin 1200 mg/1	Tablet, Extended releaseOral	AMERIFOODS TRADING COMPANY	61504-204	61504-0204-02

All 71 Mucus Relief NDCs