NDC product
Hangover Relief
NDC 61727-330 · Homeocare Laboratories
Key facts
| Product NDC | 61727-330 |
|---|---|
| Proprietary name | Hangover Relief |
| Nonproprietary name | ASAFETIDA, CAPSICUM, POTASSIUM DICHROMATE, COLA NUT, LACHESIS MUTA VENOM, STRYCHNOS NUX-VOMICA SEED, RANUNCULUS BULBOSUS, SULFURIC ACID, ZINC. |
| Substances | ASAFETIDA, CAPSICUM, POTASSIUM DICHROMATE, COLA NUT, LACHESIS MUTA VENOM, STRYCHNOS NUX-VOMICA SEED, RANUNCULUS BULBOSUS, SULFURIC ACID, ZINC |
| Dosage form | PELLET |
| Route | SUBLINGUAL |
| Labeler | Homeocare Laboratories |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [EPC] and 4 more |
| Marketing start | Nov 23, 2011 |
| Listing certified through | Dec 31, 2026 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: