The Pharma C Company Medicated Foam with Witch Hazel
- Product NDC
- 55239-358
- 11-digit product format
- 552390358
- Labeler code
- 55239
- Product ID
- 55239-358_09c37c1c-308b-6d9f-e063-6394a90a5de3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- WITCH HAZEL
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Kleen Test Products Corporation
- Application
- M015
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-05-15
- Substance
- WITCH HAZEL
- Active strength
- 500 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
- The Pharma C Company Medicated Foam with Witch Hazel
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| WITCH HAZEL | 500 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 101I4J0U34 |
| Rxcui | 2166922 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 55239-358-00 | The Pharma C Company Medicated Foam with Witch Hazel | 210 mL in 1 BOTTLE | LIQUID | 210 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55239-358 | THE PHARMA C COMPANY MEDICATED FOAM WITH WITCH HAZEL (WITCH HAZEL) LIQUID [KLEEN TEST PRODUCTS CORPORATION] | 3 | Current NDC, Legacy NDC, 1 package rows | 20231110_1a1fbe83-be45-4654-a7bb-e934e1ccd0c6.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 |
|---|
| 55239-358-00 | 55239035800 | 210 mL in 1 BOTTLE (55239-358-00) | 210 ml | 2022-05-15 | 0000-00-00 | No | No | Current |