PURELL Advanced Hand Sanitizer Green Certified Foam
NDC 21749-808, alcohol, liquid, from GOJO Industries, LLC.
- Product NDC
- 21749-808
- Status
- Listed
- Labeler
- GOJO Industries, LLC
- Dosage form
- LIQUID
- Route
- TOPICAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- OTC MONOGRAPH DRUG
- Application
- 505G(a)(3)
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/21749-808 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ALCOHOL.7 mL/mL
| Package NDC | NDC-11 | Package |
|---|---|---|
| 21749-808-51 | 21749080851 | 550 mL in 1 BOTTLE (21749-808-51) |
| 21749-808-53 | 21749080853 | 535 mL in 1 BOTTLE (21749-808-53) |
| 21749-808-89 | 21749080889 | 1200 mL in 1 BOTTLE (21749-808-89) |
| 21749-808-97 | 21749080897 | 700 mL in 1 BOTTLE (21749-808-97) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.
Use it
Look up 21749-808 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/21749-808 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 21749-808. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.