Witch Hazel
- Product NDC
- 41520-822
- 11-digit product format
- 415200822
- Labeler code
- 41520
- Product ID
- 41520-822_50ae2321-7891-12ec-e063-6394a90a8e9e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Witch Hazel
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- American Sales Company
- Application
- M015
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2015-03-24
- 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 |
|---|
| 41520-822-43 | Witch Hazel | 473 mL in 1 BOTTLE, PLASTIC | LIQUID | 473 | | 16 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 41520-822 | WITCH HAZEL LIQUID [FOODHOLD U.S.A., LLC] | 13 | Current NDC, Legacy NDC, 1 package rows | 20240907_c50d0496-6f09-43c2-9383-3250885968c9.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 |
|---|
| 41520-822-43 | 41520082243 | 473 mL in 1 BOTTLE, PLASTIC (41520-822-43) | 473 ml | 2015-03-24 | 0000-00-00 | No | No | Current |