Witch Hazel
- Product NDC
- 11822-0822
- 11-digit product format
- 118220822
- Labeler code
- 11822
- Product ID
- 11822-0822_5071426c-961c-40d1-84de-66c8ebc228eb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- WITCH HAZEL
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Rite Aid
- Application
- part347
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 1989-08-15
- Marketing end
- 0000-00-00
- Substance
- WITCH HAZEL
- Active strength
- 86 kg/100L
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 11822-0822 | D | Discontinued by firm | 2026-07-31 | ||
| excluded package | package | 11822-0822 | 11822-0822-3 | D | Discontinued by firm | 2026-07-31 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| WITCH HAZEL | ACTIVE INGREDIENT | 101I4J0U34 | WITCH HAZEL LIQUID [RITE AID] | 1 | |
| WITCH HAZEL | ACTIVE MOIETY | 101I4J0U34 | WITCH HAZEL LIQUID [RITE AID] | 1 | |
| ALCOHOL | INACTIVE INGREDIENT | 3K9958V90M | WITCH HAZEL LIQUID [RITE AID] | 1 |