Hangover Relief NDC 61727-330

NDC codes

FDA NDC Directory

Product NDC (as listed)61727-330Labeler and product segments. Claims need a package NDC.

Product NDC at billing width61727-0330Add 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
61727-330-21	61727033021	4 g in 1 TUBE (61727-330-21)Marketed from Nov 23, 2011

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): Hangover Relief
Generic name (nonproprietary): asafetida,capsicum,potassium dichromate,cola nut,lachesis muta venom,strychnos nux-vomica seed,ranunculus bulbosus,sulfuric acid,zinc.
Active ingredients: Asafetida — 5 [hp_C]/4gCapsicum — 5 [hp_C]/4gPotassium dichromate — 5 [hp_C]/4gCola nut — 5 [hp_C]/4gLachesis muta venom — 5 [hp_C]/4gStrychnos nux-vomica seed — 5 [hp_C]/4gRanunculus bulbosus — 7 [hp_C]/4gSulfuric acid — 5 [hp_C]/4gZinc — 5 [hp_C]/4g
Dosage form: Pellet
Route: Sublingual
Labeler: Homeocare Laboratories
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Nov 23, 2011
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)Vegetable Proteins (Chemical structure)
Identifiers: Product ID 61727-330_7d538d9b-6a91-ffe3-e053-2a91aa0a8f47SPL ID 7d538d9b-6a91-ffe3-e053-2a91aa0a8f47SPL set ID 93b4a184-572c-48ef-9fc0-8e357a1e0d1bUNII W9FZA51AS1, 00UK7646FG, T4423S18FM, PQM9SA369U, VSW71SS07I, 269XH13919, AEQ8NXJ0MB, O40UQP6WCF, J41CSQ7QDSUPC 0361727330215
Pharmacologic class: Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract

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. Sublingual products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N461727033021 followed by a unit qualifier and the quantity

Package 61727-0330-21. 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 18, 2018.

Indications (excerpt from the label)

Uses: For the temporary relief of headache, nausea and vomiting associated with alcohol consumption.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)