Mango
- Product NDC
- 57691-566
- 11-digit product format
- 576910566
- Labeler code
- 57691
- Product ID
- 57691-566_89ea9829-df30-455c-8450-a27204d9f71c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Alcohol
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- The Body Shop Wake Forest
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2010-09-15
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL
- Active strength
- 1 g/mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 57691-566-60 | Mango Antibacterial Hand Sanitizer | 60 mL in 1 BOTTLE | GEL | 60 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 57691-566 | MANGO (ALCOHOL) GEL [THE BODY SHOP WAKE FOREST] | 1 | Legacy NDC, 1 package rows | 20100915_d541208d-f6ec-47e0-9fc3-75c6842b5e63.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 57691-566-60 | 57691056660 | 60 mL in 1 BOTTLE | 60 ml | Historical |