Purell
- Product NDC
- 67751-188
- 11-digit product format
- 677510188
- Labeler code
- 67751
- Product ID
- 67751-188_2386259c-c602-a1c9-e063-6394a90ab73e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ALCOHOL
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Navajo Manufacturing Company Inc.
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2017-12-04
- Substance
- ALCOHOL
- Active strength
- 70 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
- Purell
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALCOHOL | 70 mL/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3K9958V90M |
| Rxcui | 581662 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67751-188-01 | Purell | 30 mL in 1 BOTTLE | GEL | 30 | | 4 |
| 67751-188-02 | Purell | 59 mL in 1 BOTTLE | GEL | 59 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67751-188 | PURELL (ALCOHOL) GEL [NAVAJO MANUFACTURING COMPANY INC.] | 4 | Current NDC, Legacy NDC, 2 package rows | 20241004_969b2968-8497-4125-949a-6be39b132edb.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 |
|---|
| 67751-188-01 | 67751018801 | 30 mL in 1 BOTTLE (67751-188-01) | 30 ml | 2017-12-04 | 0000-00-00 | No | No | Current |
| 67751-188-02 | 67751018802 | 59 mL in 1 BOTTLE (67751-188-02) | 59 ml | 2017-12-04 | 2021-09-01 | No | No | Current |