Allergy Relief
- Product NDC
- 0363-1799
- 11-digit product format
- 003631799
- Labeler code
- 0363
- Product ID
- 0363-1799_a078e904-9510-48d2-9cf4-c7786dc9b443
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Diphenhydramine HCl
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Walgreen Company
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-06-02
- Substance
- DIPHENHYDRAMINE HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| TC2D6JAD40 | DIPHENHYDRAMINE HYDROCHLORIDE | 147-24-0 | DIPHENHYDRAMINE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 0363-1799-08 | 00363179908 | 2 BLISTER PACK in 1 CARTON (0363-1799-08) / 12 TABLET, FILM COATED in 1 BLISTER PACK | 2 blister pack | 2025-06-02 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Walgreens 44-799 | Walgreen Company | LNK International, Inc. | 2025-06-02 | HUMAN OTC DRUG LABEL | 3 |