Witch Hazel
- Product NDC
- 82645-903
- 11-digit product format
- 826450903
- Labeler code
- 82645
- Product ID
- 82645-903_0d1cdfd7-c2cd-9fd5-e063-6394a90a8eda
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Witch Hazel
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Pharma Nobis, LLC
- Application
- M017
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2016-01-01
- Substance
- WITCH HAZEL
- Active strength
- 855 mg/mL
- 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 | 855 mg/mL |
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 |
|---|
| 82645-903-16 | Witch Hazel | 473 mL in 1 BOTTLE | LIQUID | 473 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 82645-903 | WITCH HAZEL LIQUID [PHARMA NOBIS, LLC] | 2 | Current NDC, Legacy NDC, 1 package rows | 20231223_e42f484d-a644-3489-e053-2a95a90a4254.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 82645-903-16 | 82645090316 | 473 mL in 1 BOTTLE (82645-903-16) | 473 ml | 2016-01-01 | 0000-00-00 | No | No | Current |