Purell Advanced Moisturizing 2in1
- Product NDC
- 21749-751
- 11-digit product format
- 217490751
- Labeler code
- 21749
- Product ID
- 21749-751_29010b40-4096-8ea3-e063-6394a90a50f2
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- alcohol
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- GOJO Industries, Inc.
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-01-25
- Substance
- ALCOHOL
- Active strength
- 70 mL/100mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
openFDA Listing Details
- Product ID
- 21749-751_29010b40-4096-8ea3-e063-6394a90a50f2
- SPL ID
- 29010b40-4096-8ea3-e063-6394a90a50f2
- Product type
- HUMAN OTC DRUG
- Finished product
- Yes
- Brand name base
- Purell Advanced Moisturizing 2in1
- Generic name
- alcohol
- Dosage form
- GEL
- Route
- TOPICAL
- Marketing start
- 2021-01-25
- Marketing category
- OTC MONOGRAPH DRUG
- Application number
- 505G(a)(3)
- Listing expiration
- 2026-12-31
openFDA Active Ingredients
| Ingredient | Strength |
|---|
| ALCOHOL | 70 mL/100mL |
openFDA Harmonized Identifiers
| Field | Values |
|---|
| Unii | 3K9958V90M |
| Rxcui | 581662 |
| Spl Set Id | 950002ed-f3a2-4ede-98fe-762ee9f018b9 |
| Manufacturer Name | GOJO Industries, Inc. |
openFDA Package Details
| Package NDC | Description | Marketing start | Sample |
|---|
| 21749-751-04 | 118 mL in 1 BOTTLE (21749-751-04) | 2021-01-25 | No |
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 3K9958V90M | ALCOHOL | 64-17-5 | ALCOHOL |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 21749-751-04 | 21749075104 | 118 mL in 1 BOTTLE (21749-751-04) | 118 ml | 2021-01-25 | No | No | Historical |