Hand Sanitizer Foam
- Product NDC
- 72471-100
- 11-digit product format
- 724710100
- Labeler code
- 72471
- Product ID
- 72471-100_d626aba9-5956-4a05-e053-2995a90a82d9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Anti-bacterial Advanced Formula
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- VMP Cosmetics, LLC
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-07-20
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 0 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72471-100-20 | Hand Sanitizer Foam | 1 g in 1 BOTTLE, PLASTIC | LIQUID | 1 | | 3 |
| 72471-100-21 | Hand Sanitizer Foam | 1 g in 1 BOTTLE, PLASTIC | LIQUID | 1 | | 3 |
| 72471-100-22 | Hand Sanitizer Foam | 1 g in 1 BOTTLE, PLASTIC | LIQUID | 1 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72471-100 | HAND SANITIZER FOAM (ANTI-BACTERIAL ADVANCED FORMULA) LIQUID [VMP COSMETICS, LLC] | 3 | Legacy NDC, 3 package rows | 20220123_aabc441a-89ef-2bf8-e053-2a95a90aba2d.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 |
|---|
| 72471-100-20 | 72471010020 | 1 g in 1 BOTTLE, PLASTIC (72471-100-20) | 1 g | 2020-07-20 | 0000-00-00 | No | No | Current |
| 72471-100-21 | 72471010021 | 1 g in 1 BOTTLE, PLASTIC (72471-100-21) | 1 g | 2020-09-18 | 0000-00-00 | No | No | Current |
| 72471-100-22 | 72471010022 | 1 g in 1 BOTTLE, PLASTIC (72471-100-22) | 1 g | 2020-09-18 | 0000-00-00 | No | No | Current |