7th MANNA PAIN RELIEF DROPS NDC 71856-423

NDC codes

FDA NDC Directory

Product NDC (as listed)71856-423Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71856-0423Add 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
71856-423-00	71856042300	1 BOTTLE in 1 BOX (71856-423-00) / 30 mL in 1 BOTTLEMarketed from Sep 25, 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): 7th MANNA PAIN RELIEF DROPS
Generic name (nonproprietary): menthol, camphor (synthetic)
Active ingredients: Menthol — 100 mg/mLCamphor (Synthetic) — 30 mg/mL
Dosage form: Liquid
Route: Topical
Labeler: 7TH MANNA (USA) PTE. LTD.
Product type: Over-the-counter drug
Marketing category: OTC monograph drugApplication M017B
Marketing start: Sep 25, 2023
Listing expires: Dec 31, 2026
Identifiers: Product ID 71856-423_09dc19d0-24b9-bd12-e063-6294a90ab40fSPL ID 09dc19d0-24b9-bd12-e063-6294a90ab40fSPL set ID 699c668c-4f54-4f18-b585-bdcebe7a2c4eRxCUI 1987413UNII L7T10EIP3A, 5TJD82A1ET

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

N471856042300 followed by a unit qualifier and the quantity

Package 71856-0423-00. 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 Nov 11, 2023.

Indications (excerpt from the label)

Uses For the temporary relief of minor aches and pains of muscles and joints associated with: arthritis sprains strains bruises simple backaches

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)