Antimicrobial Hand
- Product NDC
- 77617-008
- 11-digit product format
- 776170008
- Labeler code
- 77617
- Product ID
- 77617-008_47a13236-aee7-49d9-9b93-d98126f3bf1b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Maintex
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2018-04-15
- Marketing end
- 2022-11-18
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 13 kg/100kg
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 77617-008-02 | 77617000802 | 1 BOTTLE, PLASTIC in 1 BOX (77617-008-02) > 3.80564 kg in 1 BOTTLE, PLASTIC (77617-008-01) | 2018-04-15 | 2022-11-18 | No | No | Current |