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
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 |
|---|
| 68210-4218-3 | Allergy Relief | 300 in 1 JAR | TABLET, FILM COATED | 300 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68210-4218 | ALLERGY RELIEF (DIPHENHYDRAIME HCL) TABLET, FILM COATED [SPIRIT PHARMACEUTICALS LLC] | 4 | Legacy NDC, 1 package rows | 20241211_99ca3ec9-a28d-4851-951d-34aa982de9d8.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| 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 |