Allergy Relief
- Product NDC
- 68210-4218
- 11-digit product format
- 682104218
- Labeler code
- 68210
- Product ID
- 68210-4218_ed71ecb2-6be5-a180-e053-2a95a90a2393
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Diphenhydraime HCl
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Spirit Pharmaceuticals LLC
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2022-11-14
- 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
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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68210-4218-3 | 68210421803 | 300 TABLET, FILM COATED in 1 JAR (68210-4218-3) | 2022-11-14 | 0000-00-00 | No | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Allergy Relief | Spirit Pharmaceuticals LLC | 2024-12-09 | HUMAN OTC DRUG LABEL | 4 |