Wet wipes
- Product NDC
- 75213-001
- Requested package NDC
- 75213-001-10
- 11-digit product format
- 752130001
- Labeler code
- 75213
- Product ID
- 75213-001_eb755f07-c61c-812f-e053-2a95a90adc3c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride,Didecyldimonium Chloride
- Dosage form
- SWAB
- Route
- TOPICAL
- Labeler
- Hangzhou LUC Travel Products Co., LTD.
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-03-21
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE; DIDECYLDIMONIUM CHLORIDE
- Active strength
- 0 g/100g; g/100g
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 75213-001-10 | 75213000110 | 12 PAIL in 1 CARTON (75213-001-10) > 150 POUCH in 1 PAIL > .54 g in 1 POUCH | 12 pail | 2020-03-21 | 0000-00-00 | No | No | Current |