Childrens Allergy
- Product NDC
- 11822-0020
- Requested package NDC
- 11822-0020-6
- 11-digit product format
- 118220020
- Labeler code
- 11822
- Product ID
- 11822-0020_334e4681-39cd-4a9f-957b-7088bc9d4d4d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Diphenhydramine Hydrochloride
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Rite Aid Corporation
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2021-01-29
- 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.
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11822-0020 | CHILDRENS ALLERGY (DIPHENHYDRAMINE HYDROCHLORIDE) LIQUID [RITE AID CORPORATION] | 4 | Legacy NDC | 20241109_50900520-82df-4ec6-85b9-573ee910c79a.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11822-0020-6 | 11822002006 | 1 BOTTLE, PLASTIC in 1 BOX (11822-0020-6) > 237 mL in 1 BOTTLE, PLASTIC | 2021-01-29 | 0000-00-00 | No | No | Current |