MANUGEL 85
- Product NDC
- 62169-202
- 11-digit product format
- 621690202
- Labeler code
- 62169
- Product ID
- 62169-202_35842aa1-812f-42c1-a7bf-3a40e58ddfee
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Ethanol
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Laboratoires Anios
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2014-04-01
- Marketing end
- 0000-00-00
- Substance
- ALCOHOL; PHENOXYETHANOL
- Active strength
- 400 mL/500mL; g/500mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 62169-202-12 | MANUGEL 85 | 12 in 1 PACKAGE | GEL | 12 | | 3 |
| 62169-202-17 | MANUGEL 85 | 500 mL in 1 BOTTLE, PLASTIC | GEL | 500 | | 3 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62169-202 | MANUGEL 85 (ETHANOL) GEL [LABORATOIRES ANIOS] | 3 | Legacy NDC, 2 package rows | 20140402_5b980767-7a5a-4674-96c5-78cf206cd463.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 62169-202-12 | 62169020212 | 12 in 1 PACKAGE | | Historical |
| 62169-202-17 | 62169020217 | 500 mL in 1 BOTTLE, PLASTIC | 500 ml | Historical |