Wet wipes
- Product NDC
- 75213-002
- Requested package NDC
- 75213-002-01
- 11-digit product format
- 752130002
- Labeler code
- 75213
- Product ID
- 75213-002_eb756030-a112-a7da-e053-2a95a90a08f4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- SWAB
- Route
- TOPICAL
- Labeler
- Hangzhou LUC Travel Products Co., LTD.
- Application
- part333A
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-05-29
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 0 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 75213-002-01 | 75213000201 | 100 BAG in 1 CARTON (75213-002-01) > 10 POUCH in 1 BAG > .005265 g in 1 POUCH | 100 bag | 2020-05-29 | 0000-00-00 | No | No | Current |