Hand Sanitizer
- Product NDC
- 72131-002
- 11-digit product format
- 721310002
- Labeler code
- 72131
- Product ID
- 72131-002_676f6b7c-2971-10e5-e053-2991aa0aecb0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BENZETHONIUM CHLORIDE
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- RIMPORTS INC.
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2018-03-06
- Marketing end
- 0000-00-00
- Substance
- BENZETHONIUM CHLORIDE
- Active strength
- 0 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
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 |
|---|
| 72131-002-01 | Hand Sanitizer | 59 mL in 1 BOTTLE, PLASTIC | GEL | 59 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72131-002 | HAND SANITIZER (BENZETHONIUM CHLORIDE) GEL [RIMPORTS INC.] | 2 | Legacy NDC, 1 package rows | 20180315_676c3b3b-86e3-c4b6-e053-2a91aa0acbd6.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 72131-002-01 | 72131000201 | 59 mL in 1 BOTTLE, PLASTIC | 59 ml | Historical |