Witch Hazel
- Product NDC
- 49580-0390
- 11-digit product format
- 495800390
- Labeler code
- 49580
- Product ID
- 49580-0390_7d907ebf-e5b0-42d7-96e5-98a19b5449e3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Witch hazel
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- P & L Development, LLC
- Application
- M016
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2014-08-31
- Substance
- WITCH HAZEL
- Active strength
- 86 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
- Witch Hazel
- Brand name suffix
- ReadyInCase
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| WITCH HAZEL | 86 g/100mL |
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 |
|---|
| 49580-0390-6 | Witch HazelReadyInCase | 473 mL in 1 BOTTLE, PLASTIC | LIQUID | 473 | | 7 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 49580-0390 | WITCH HAZEL READYINCASE (WITCH HAZEL) LIQUID [P & L DEVELOPMENT, LLC] | 7 | Current NDC, Legacy NDC, 1 package rows | 20250214_1588244a-c9e8-4a04-b605-10e35c225e6c.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 |
|---|
| 49580-0390-6 | 49580039006 | 473 mL in 1 BOTTLE, PLASTIC (49580-0390-6) | 473 ml | 2014-08-31 | 0000-00-00 | No | No | Current |