Witch Hazel
- Product NDC
- 41250-822
- 11-digit product format
- 412500822
- Labeler code
- 41250
- Product ID
- 41250-822_4b34762c-db2f-f8ba-e063-6394a90a273d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- WITCH HAZEL
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Meijer, Inc.
- Application
- M016
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 1996-03-15
- Substance
- WITCH HAZEL
- Active strength
- 86 kg/100L
- 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 | 86 kg/100L |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 101I4J0U34 |
| Rxcui | 200295 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 41250-822-43 | Witch Hazel | 0.473 L in 1 BOTTLE, PLASTIC | LIQUID | 0.473 | | 20 |
| 41250-822-99 | Witch Hazel | 0.236 L in 1 BOTTLE, PUMP | LIQUID | 0.236 | | 20 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 41250-822 | WITCH HAZEL LIQUID [MEIJER DISTRIBUTION, INC] | 18 | Current NDC, Legacy NDC, 2 package rows | 20241114_13e4aece-5b91-4f89-a912-540bf170a8d1.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 41250-822-43 | 41250082243 | .473 L in 1 BOTTLE, PLASTIC (41250-822-43) | 1996-03-15 | 0000-00-00 | No | No | Current |
| 41250-822-99 | 41250082299 | .236 L in 1 BOTTLE, PUMP (41250-822-99) | 1996-03-15 | 0000-00-00 | No | No | Current |