Witch Hazel
- Product NDC
- 76162-822
- 11-digit product format
- 761620822
- Labeler code
- 76162
- Product ID
- 76162-822_4ab9bfe0-d6b8-9473-e063-6294a90ad884
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- WITCH HAZEL
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Topco Associates LLC
- Application
- M016
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2019-03-08
- Substance
- WITCH HAZEL
- Active strength
- 860 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Witch Hazel
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| WITCH HAZEL | 860 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 101I4J0U34 |
| Rxcui | 200295 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 76162-822-43 | Witch Hazel | 473 mL in 1 BOTTLE, PLASTIC | LIQUID | 473 | | 9 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 76162-822 | WITCH HAZEL LIQUID [TOPCO ASSOCIATES LLC] | 8 | Current NDC, Legacy NDC, 1 package rows | 20250322_471a9f8d-ba12-41d3-a510-20c1a13ff850.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 76162-822-43 | 76162082243 | 473 mL in 1 BOTTLE, PLASTIC (76162-822-43) | 473 ml | 2019-03-08 | 0000-00-00 | No | No | Current |