Hand Sanitizer
- Product NDC
- 78695-534
- 11-digit product format
- 786950534
- Labeler code
- 78695
- Product ID
- 78695-534_a75b180d-44ee-b972-e053-2a95a90a3ea7
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALCOHOL
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- St. Petersburg Distillery Company, LLC
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-03-30
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 80 mL/100mL
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 78695-534-08 | Hand Sanitizer | 50 mL in 1 BOTTLE | LIQUID | 50 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 78695-534 | HAND SANITIZER (ALCOHOL) LIQUID [ST. PETERSBURG DISTILLERY COMPANY, LLC] | 1 | Legacy NDC, 1 package rows | 20200625_a75b1da6-3a83-0579-e053-2995a90a271c.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 |
|---|
| 78695-534-08 | 78695053408 | 50 mL in 1 BOTTLE (78695-534-08) | 50 ml | 2020-03-30 | 0000-00-00 | No | No | Current |