Hand Sanitizer
- Product NDC
- 77839-123
- 11-digit product format
- 778390123
- Labeler code
- 77839
- Product ID
- 77839-123_a9f39618-44bf-4b7c-e053-2995a90a55de
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALCOHOL
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- RMS International (USA) Inc.
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-03-30
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 74 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 |
|---|
| 77839-123-45 | Hand Sanitizer | 30 mL in 1 BOX | LIQUID | 30 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 77839-123 | HAND SANITIZER (ALCOHOL) LIQUID [RMS INTERNATIONAL (USA) INC.] | 3 | Legacy NDC, 1 package rows | 20200709_a58b3821-3b67-0add-e053-2995a90a0e06.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 |
|---|
| 77839-123-45 | 77839012345 | 30 mL in 1 BOX (77839-123-45) | 30 ml | 2020-07-13 | 0000-00-00 | No | No | Current |