ALLERGY RELIEF
- Product NDC
- 36800-669
- Requested package NDC
- 36800-669-10
- 11-digit product format
- 368000669
- Labeler code
- 36800
- Product ID
- 36800-669_ee288a89-8dfb-29cf-e053-2a95a90a0a80
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- DIPHENHYDRAMINE HYDROCHLORIDE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- TOPCO ASSOCIATES LLC
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2021-08-10
- Marketing end
- 0000-00-00
- 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
- 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.
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 36800-669-10 | ALLERGY RELIEF | 1 in 1 CARTON | TABLET, FILM COATED | 1 | | 7 |
| 36800-669-10 | ALLERGY RELIEF | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 36800-669 | ALLERGY RELIEF (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET, FILM COATED [TOPCO ASSOCIATES LLC] | 7 | Legacy NDC, 2 package rows | 20250101_ad676e67-4cdd-41bb-8bd8-0c5868539fea.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 36800-669-10 | 36800066910 | 1 BOTTLE in 1 CARTON (36800-669-10) > 100 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2021-08-10 | 0000-00-00 | No | No | Current |