Honey Pot
- Product NDC
- 71505-022
- 11-digit product format
- 715050022
- Labeler code
- 71505
- Product ID
- 71505-022_ddc4f5ad-9ed8-cc1a-e053-2a95a90a8668
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Anti-Itch Soothing
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Disposable Hygiene LLC dba Anthem
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2022-02-15
- Marketing end
- 0000-00-00
- Substance
- PRAMOXINE HYDROCHLORIDE
- Active strength
- 10 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 71505-022-80 | Honey Pot | 80 mL in 1 BOTTLE | LIQUID | 80 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71505-022 | HONEY POT (ANTI-ITCH SOOTHING) LIQUID [DISPOSABLE HYGIENE LLC DBA ANTHEM] | 1 | Legacy NDC, 1 package rows | 20220429_ddc4f5ad-9ed9-cc1a-e053-2a95a90a8668.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 |
|---|
| 71505-022-80 | 71505002280 | 80 mL in 1 BOTTLE (71505-022-80) | 80 ml | 2022-02-15 | 0000-00-00 | No | No | Current |