rexall sleep aid
- Product NDC
- 55910-702
- 11-digit product format
- 559100702
- Labeler code
- 55910
- Product ID
- 55910-702_af12b140-704c-45c4-800a-2aea2814faee
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Diphenhydramine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Dolgencorp, LLC
- Application
- part338
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2010-09-29
- Marketing end
- 0000-00-00
- Substance
- DIPHENHYDRAMINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 55910-702 | D | Discontinued by firm | 2026-10-12 | ||
| excluded package | package | 55910-702 | 55910-702-78 | D | Discontinued by firm | 2026-10-12 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 55910-702-78 | 55910070278 | 1 BOTTLE in 1 CARTON (55910-702-78) > 100 TABLET in 1 BOTTLE | 1 bottle | 2010-09-29 | 0000-00-00 | No | No | Current |