Antibacterial Hand Wipes
- Product NDC
- 67751-232
- 11-digit product format
- 677510232
- Labeler code
- 67751
- Product ID
- 67751-232_2abd75c3-5552-d428-e063-6294a90ae77d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- benzalkonium chloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Navajo Manufacturing Company Inc.
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-05-01
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- .13 g/100g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67751-232-15 | Antibacterial Hand Wipes | 15 in 1 PACKAGE | LIQUID | 15 | | 3 |
| 67751-232-15 | Antibacterial Hand Wipes | 4.2 g in 1 POUCH | LIQUID | 4.2 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67751-232 | ANTIBACTERIAL HAND WIPES (BENZALKONIUM CHLORIDE) LIQUID [NAVAJO MANUFACTURING COMPANY INC.] | 3 | Current NDC, 2 package rows | 20250104_15aee3b6-1387-81df-e063-6294a90ae3ed.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 67751-232-15 | 67751023215 | 15 POUCH in 1 PACKAGE (67751-232-15) / 4.2 g in 1 POUCH | 15 pouch | 2020-05-01 | No | No | Historical |