PURELL Antimicrobial Foaming Hand
- Product NDC
- 21749-610
- 11-digit product format
- 217490610
- Labeler code
- 21749
- Product ID
- 21749-610_2a976ebe-2fd0-a496-e063-6294a90a2dae
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- GOJO Industries, Inc.
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-12-11
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- .5 mg/100mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- PURELL Antimicrobial Foaming Hand
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZALKONIUM CHLORIDE | .5 mg/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | F5UM2KM3W7 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 21749-610-40 | PURELL Antimicrobial Foaming Hand | 1200 mL in 1 PACKAGE | LIQUID | 1200 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21749-610 | PURELL ANTIMICROBIAL FOAMING HAND (BENZALKONIUM CHLORIDE) LIQUID [GOJO INDUSTRIES, INC.] | 2 | Current NDC, 1 package rows | 20250101_fd5d9942-1cd3-4c40-84bf-beb432768219.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 21749-610-40 | 21749061040 | 1200 mL in 1 PACKAGE (21749-610-40) | 1200 ml | 2023-12-11 | No | No | Current |