Benadryl
- Product NDC
- 66715-6406
- 11-digit product format
- 667156406
- Labeler code
- 66715
- Product ID
- 66715-6406_2783d396-2842-91e9-e063-6294a90a88fe
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Diphenhydramine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Lil' Drug Store Products, Inc.
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-04-19
- 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
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 |
|---|
| 66715-6406-2 | 66715640602 | 2 POUCH in 1 CARTON (66715-6406-2) / 2 TABLET, FILM COATED in 1 POUCH | 2 pouch | 2022-11-28 | No | No | Historical |
| 66715-6406-7 | 66715640607 | 25 POUCH in 1 BOX, UNIT-DOSE (66715-6406-7) / 2 TABLET, FILM COATED in 1 POUCH | 25 pouch | 2022-04-19 | No | No | Historical |
| 66715-6406-8 | 66715640608 | 30 POUCH in 1 BOX, UNIT-DOSE (66715-6406-8) / 2 TABLET, FILM COATED in 1 POUCH | 30 pouch | 2022-04-19 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Benadryl ® | Lil' Drug Store Products, Inc. | 2024-11-22 | HUMAN OTC DRUG LABEL | 10 |
| Benadryl ® | Lil' Drug Store Products, Inc. | 2023-09-26 | HUMAN OTC DRUG LABEL | 9 |