ProGel Max Hand Sanitizer
- Product NDC
- 66353-117
- 11-digit product format
- 663530117
- Labeler code
- 66353
- Product ID
- 66353-117_249e095b-fba3-b6a2-e063-6394a90a7459
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALCOHOL
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Delta Pharma Inc.
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-06-12
- Substance
- ALCOHOL
- Active strength
- 80 mL/100mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- ProGel Max Hand Sanitizer
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALCOHOL | 80 mL/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3K9958V90M |
| Rxcui | 1039339 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 66353-117-01 | ProGel Max Hand Sanitizer | 350 mL in 1 BOTTLE | LIQUID | 350 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 66353-117 | PROGEL MAX HAND SANITIZER (ALCOHOL) LIQUID [DELTA PHARMA INC.] | 2 | Current NDC, Legacy NDC, 1 package rows | 20241018_a607897c-c398-1931-e053-2a95a90ae483.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 |
|---|
| 66353-117-01 | 66353011701 | 350 mL in 1 BOTTLE (66353-117-01) | 350 ml | 2020-06-12 | 0000-00-00 | No | No | Current |