Witch Hazel
- Product NDC
- 56104-904
- 11-digit product format
- 561040904
- Labeler code
- 56104
- Product ID
- 56104-904_42b885ee-203a-2e7a-e063-6394a90ad29b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Witch Hazel
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Premier Brands of America Inc.
- Application
- M016
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-08-27
- Substance
- WITCH HAZEL
- Active strength
- 860 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Witch Hazel
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| WITCH HAZEL | 860 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 101I4J0U34 |
| Rxcui | 1987674 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 56104-904-01 | Witch Hazel | 170 g in 1 CAN | SPRAY | 170 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 56104-904-01 | 56104090401 | 170 g in 1 CAN (56104-904-01) | 170 g | 2025-06-23 | No | No | Current |