Private Label Poison Ivy Wash
- Product NDC
- 0802-0119
- 11-digit product format
- 008020119
- Labeler code
- 0802
- Product ID
- 0802-0119_a8862995-5d80-64a6-e053-2a95a90a6ebe
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Pramoxine Hydrochloride
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Humco Holding Group, Inc.
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2018-06-18
- Marketing end
- 0000-00-00
- Substance
- PRAMOXINE HYDROCHLORIDE
- Active strength
- 1 mg/mg
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0802-0119-96 | Private Label Poison Ivy Wash | 117000 mg in 1 BOTTLE | LOTION | 117000 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0802-0119 | PRIVATE LABEL POISON IVY WASH (PRAMOXINE HYDROCHLORIDE) LOTION [HUMCO HOLDING GROUP, INC.] | 2 | Legacy NDC, 1 package rows | 20200622_6eeebc09-309a-2283-e053-2991aa0acbf6.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 |
|---|
| 0802-0119-96 | 00802011996 | 117000 mg in 1 BOTTLE (0802-0119-96) | 117000 mg | 2018-06-18 | 0000-00-00 | No | No | Current |