AQUACOOL MULTI 500
- Product NDC
- 70759-0012
- 11-digit product format
- 707590012
- Labeler code
- 70759
- Product ID
- 70759-0012_60d16dbe-4dd6-a9f5-e053-2991aa0a4629
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- MENTHOL
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Pharmanuco
- Application
- part348
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2017-12-01
- Marketing end
- 0000-00-00
- Substance
- MENTHOL
- Active strength
- 3 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 70759-0012-1 | AQUACOOL MULTI 500 | 500 mL in 1 BOTTLE, PUMP | GEL | 500 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70759-0012 | AQUACOOL MULTI 500 (MENTHOL) GEL [PHARMANUCO] | 1 | Legacy NDC, 1 package rows | 20171221_60d16dbe-4dd5-a9f5-e053-2991aa0a4629.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 70759-0012-1 | 70759001201 | 500 mL in 1 BOTTLE, PUMP | 500 ml | Historical |