Benadryl Allergy
- Product NDC
- 50269-528
- 11-digit product format
- 502690528
- Labeler code
- 50269
- Product ID
- 50269-528_3de8c1da-4aaf-e1f7-e063-6294a90ae112
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- DIPHENHYDRAMINE HYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- JC World Bell Wholesale Co., Inc.
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2012-06-04
- 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 Allergy
- 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 |
|---|
| 50269-528-00 | Benadryl Allergy | 20 in 1 POUCH | TABLET, FILM COATED | 20 | | 1 |
| 50269-528-00 | Benadryl Allergy | 2 in 1 BOX | TABLET, FILM COATED | 2 | | 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 |
|---|
| 50269-528-00 | 50269052800 | 2 POUCH in 1 BOX (50269-528-00) / 20 TABLET, FILM COATED in 1 POUCH | 2 pouch | 2012-06-04 | No | No | Historical |