ACQUAINT Antibacterial Foam Handwash
- Product NDC
- 21749-551
- 11-digit product format
- 217490551
- Labeler code
- 21749
- Product ID
- 21749-551_284d5bbf-dd60-99a2-e063-6394a90a3600
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Chloroxylenol
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- GOJO Industries, Inc.
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2004-09-09
- Substance
- CHLOROXYLENOL
- Active strength
- .003 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- ACQUAINT Antibacterial Foam Handwash
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CHLOROXYLENOL | .003 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 0F32U78V2Q |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 21749-551-90 | ACQUAINT Antibacterial Foam Handwash | 1250 mL in 1 PACKAGE | LIQUID | 1250 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21749-551 | ACQUAINT ANTIBACTERIAL FOAM HANDWASH (CHLOROXYLENOL) LIQUID [GOJO INDUSTRIES, INC.] | 4 | Current NDC, Legacy NDC, 1 package rows | 20241204_515c40e6-2a0a-43e5-a44f-ecabace0ae10.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 21749-551-90 | 21749055190 | 1250 mL in 1 PACKAGE (21749-551-90) | 1250 ml | 2004-09-09 | 0000-00-00 | No | No | Current |