Indulgence/ProPower
- Product NDC
- 61307-213
- Requested package NDC
- 61307-213-10
- 11-digit product format
- 613070213
- Labeler code
- 61307
- Product ID
- 61307-213_f1e9f9e2-fcf0-61d2-e053-2995a90af59d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- SOAP
- Route
- TOPICAL
- Labeler
- U S Chemical Corporation
- Application
- part333E
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2017-01-30
- Marketing end
- 0000-00-00
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 3 mg/L
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- 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 |
|---|
| 61307-213-10 | 61307021310 | 1 L in 1 BAG (61307-213-10) | 1 l | 2017-01-30 | 0000-00-00 | No | No | Current |