Personal CARE
- Product NDC
- 72133-149
- 11-digit product format
- 721330149
- Labeler code
- 72133
- Product ID
- 72133-149_69ae73bf-c85b-53a2-e053-2991aa0ae18a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium chloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Delta Brands & Products LLC
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2018-04-02
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 0 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72133-149 | PERSONAL CARE FOAMING HAND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [DELTA BRANDS & PRODUCTS LLC] | 2 | Legacy NDC | 20180413_69abe1b1-3aae-d8c2-e053-2a91aa0ab89f.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72133-149-07 | 72133014907 | 207 mL in 1 BOTTLE, PUMP (72133-149-07) | 207 ml | 2018-04-02 | 0000-00-00 | No | No | Current |