Universal WITCH HAZEL
- Product NDC
- 52000-414
- 11-digit product format
- 520000414
- Labeler code
- 52000
- Product ID
- 52000-414_66486f72-a425-450d-9669-0fa18a4899ee
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- witch hazel
- Dosage form
- SOLUTION
- Route
- TOPICAL
- Labeler
- Universal Distribution Center LLC
- Application
- M016
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-07-01
- Substance
- WITCH HAZEL
- Active strength
- 3 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Universal WITCH HAZEL
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| WITCH HAZEL | 3 g/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 101I4J0U34 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 52000-414-06 | Universal WITCH HAZEL | 177 mL in 1 BOTTLE, PLASTIC | SOLUTION | 177 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 52000-414 | UNIVERSAL WITCH HAZEL (WITCH HAZEL) SOLUTION [UNIVERSAL DISTRIBUTION CENTER LLC] | 2 | Current NDC, 1 package rows | 20241215_7e0b56ef-fa41-4862-b387-5b58d81d67d4.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 52000-414-06 | 52000041406 | 177 mL in 1 BOTTLE, PLASTIC (52000-414-06) | 177 ml | 2023-07-01 | No | No | Current |