Hangover Relief
- Product NDC
- 61727-330
- 11-digit product format
- 617270330
- Labeler code
- 61727
- Product ID
- 61727-330_7d538d9b-6a91-ffe3-e053-2a91aa0a8f47
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- 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
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2011-11-23
- Substance
- ASAFETIDA; CAPSICUM; COLA NUT; LACHESIS MUTA VENOM; POTASSIUM DICHROMATE; RANUNCULUS BULBOSUS; STRYCHNOS NUX-VOMICA SEED; SULFURIC ACID; ZINC
- Active strength
- 5; 5; 5; 5; 5; 7; 5; 5; 5 [hp_C]/4g; [hp_C]/4g; [hp_C]/4g; [hp_C]/4g; [hp_C]/4g; [hp_C]/4g; [hp_C]/4g; [hp_C]/4g; [hp_C]/4g
- Pharmacologic classes
- Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Plant Proteins [CS], Seed Storage Proteins [CS], Vegetable Proteins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Hangover Relief
- Listing expiration
- 2026-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| ASAFETIDA | 5 [hp_C]/4g |
| CAPSICUM | 5 [hp_C]/4g |
| POTASSIUM DICHROMATE | 5 [hp_C]/4g |
| COLA NUT | 5 [hp_C]/4g |
| LACHESIS MUTA VENOM | 5 [hp_C]/4g |
| STRYCHNOS NUX-VOMICA SEED | 7 [hp_C]/4g |
| RANUNCULUS BULBOSUS | 5 [hp_C]/4g |
| SULFURIC ACID | 5 [hp_C]/4g |
| ZINC | 5 [hp_C]/4g |
Harmonized UNII identifiers#
| Identifier | FDA.report destination |
|---|---|
| W9FZA51AS1 | Internal UNII lookup |
| 00UK7646FG | Internal UNII lookup |
| T4423S18FM | Internal UNII lookup |
| PQM9SA369U | Internal UNII lookup |
| VSW71SS07I | Internal UNII lookup |
| 269XH13919 | Internal UNII lookup |
| AEQ8NXJ0MB | Internal UNII lookup |
| O40UQP6WCF | Internal UNII lookup |
| J41CSQ7QDS | Internal UNII lookup |
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 93b4a184-572c-48ef-9fc0-8e357a1e0d1b | Available on FDA.report |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 61727-330-21 | Hangover Relief | 4 g in 1 TUBE | PELLET | 4 | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 61727-330 | HANGOVER RELIEF (ASAFETIDA,CAPSICUM,POTASSIUM DICHROMATE,COLA NUT,LACHESIS MUTA VENOM,STRYCHNOS NUX-VOMICA SEED,RANUNCULUS BULBOSUS,SULFURIC ACID,ZINC.) PELLET [HOMEOCARE LABORATORIES] | 2 | Current NDC, Legacy NDC, 1 package rows | 20190228_93b4a184-572c-48ef-9fc0-8e357a1e0d1b.zip |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Hangover Relief | ASAFETIDA,CAPSICUM,POTASSIUM DICHROMATE,COLA NUT,LACHESIS MUTA VENOM,STRYCHNOS NUX-VOMICA SEED,RANUNCULUS BULBOSUS,SULFURIC ACID,ZINC. | Homeocare Laboratories | 93b4a184-572c-48ef-9fc0-8e357a1e0d1b | 2018-12-18 | Warnings | 61727-330 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 61727-330-21 | 61727033021 | 4 g in 1 TUBE (61727-330-21) | 4 g | 2011-11-23 | 0000-00-00 | No | No | Current |