Childrens Allergy Relief
- Product NDC
- 70302-012
- 11-digit product format
- 703020012
- Labeler code
- 70302
- Product ID
- 70302-012_bd4b30b5-ab5a-dc24-e053-2995a90a9bd0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- DIPHENHYDRAMINE HYDROCHLORIDE
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- New Vision Pharmaceuticals LLC
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2018-11-01
- Marketing end
- 0000-00-00
- Substance
- DIPHENHYDRAMINE HYDROCHLORIDE
- Active strength
- 13 mg/5mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Packages#
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 70302-012-20 | 70302001220 | 20 VIAL, SINGLE-USE in 1 BOX (70302-012-20) > 5 mL in 1 VIAL, SINGLE-USE | 2018-11-01 | 0000-00-00 | No | No | Current |