OLIKA Ultra Hydrating Hand Sanitizer, Brave
- Product NDC
- 73517-951
- 11-digit product format
- 735170951
- Labeler code
- 73517
- Product ID
- 73517-951_de789644-1083-1ed8-e053-2995a90add68
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALCOHOL
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Amyris, Inc
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2022-05-09
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 65 mL/100mL
- 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 |
|---|
| 73517-951-02 | OLIKA Ultra Hydrating Hand Sanitizer, Brave | 20 mL in 1 BOTTLE, DISPENSING | GEL | 20 | | 2 |
| 73517-951-03 | OLIKA Ultra Hydrating Hand Sanitizer, Brave | 90 mL in 1 POUCH | GEL | 90 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 73517-951 | OLIKA ULTRA HYDRATING HAND SANITIZER, BRAVE (ALCOHOL) GEL [AMYRIS, INC] | 2 | Legacy NDC, 2 package rows | 20220509_de615637-4345-0ae1-e053-2a95a90ae9c1.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 |
|---|
| 73517-951-02 | 73517095102 | 20 mL in 1 BOTTLE, DISPENSING (73517-951-02) | 20 ml | 2022-05-09 | 0000-00-00 | No | No | Current |
| 73517-951-03 | 73517095103 | 90 mL in 1 POUCH (73517-951-03) | 90 ml | 2022-05-09 | 0000-00-00 | No | No | Current |