Benadryl
- Product NDC
- 53209-3001
- 11-digit product format
- 532093001
- Labeler code
- 53209
- Product ID
- 53209-3001_371fa3fe-9460-112b-e063-6294a90afe82
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Diphenhydramine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Morning Star OTC
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-06-09
- Substance
- DIPHENHYDRAMINE HYDROCHLORIDE
- Active strength
- 25 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Benadryl
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DIPHENHYDRAMINE HYDROCHLORIDE | 25 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | TC2D6JAD40 |
| Rxcui | 1049630, 1049632 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 53209-3001-1 | Benadryl | 2 in 1 BLISTER PACK | TABLET, FILM COATED | 2 | | 1 |
| 53209-3001-2 | Benadryl | 25 in 1 PACKET | TABLET, FILM COATED | 25 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 53209-3001-1 | 53209300101 | 2 in 1 BLISTER PACK | | | | | Historical |
| 53209-3001-2 | 53209300102 | 25 BLISTER PACK in 1 PACKET (53209-3001-2) / 2 TABLET, FILM COATED in 1 BLISTER PACK (53209-3001-1) | 25 blister pack | 2025-06-09 | No | No | Current |