Lucky
- Product NDC
- 20276-325
- Requested package NDC
- 20276-325-35
- 11-digit product format
- 202760325
- Labeler code
- 20276
- Product ID
- 20276-325_d6dd3f04-8017-8859-e053-2995a90a5ed5
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Diphenhydramine hydrochloride Zinc acetate
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Delta Brands Inc
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2014-11-15
- Marketing end
- 0000-00-00
- Substance
- DIPHENHYDRAMINE HYDROCHLORIDE; ZINC ACETATE
- Active strength
- 2 g/100g; g/100g
- Pharmacologic classes
- Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing#
DailyMed Socrata Ingredients#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 20276-325-35 | 20276032535 | 35.4 g in 1 TUBE (20276-325-35) | 35.4 g | 2020-03-01 | 0000-00-00 | No | No | Current |