Duradry
- Product NDC
- 58443-0429
- 11-digit product format
- 584430429
- Labeler code
- 58443
- Product ID
- 58443-0429_cf7052ed-2f9d-4920-e053-2a95a90ae977
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aluminum Zirconium Trichlorohydrex Gly
- Dosage form
- STICK
- Route
- TOPICAL
- Labeler
- Prime Enterprises Inc.
- Application
- part350
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2021-01-04
- Marketing end
- 0000-00-00
- Substance
- ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY
- Active strength
- 200 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 58443-0429-3 | 58443042903 | 65 g in 1 BOTTLE, PLASTIC (58443-0429-3) | 65 g | 2021-01-04 | 0000-00-00 | No | No | Current |