Gillette Clinical
- Product NDC
- 69423-157
- 11-digit product format
- 694230157
- Labeler code
- 69423
- Product ID
- 69423-157_d6957d5e-ea9c-d1f4-e053-2995a90a5b12
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aluminum Zirconium Octachlorohydrex Gly
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- The Procter & Gamble Manufacturing Company
- Application
- part350
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2016-02-02
- Marketing end
- 2023-06-15
- Substance
- ALUMINUM ZIRCONIUM OCTACHLOROHYDREX GLY
- Active strength
- 20 g/100g
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69423-157-45 | 69423015745 | 1 CANISTER in 1 CARTON (69423-157-45) > 45 g in 1 CANISTER | 1 canister | 2016-02-02 | 0000-00-00 | No | No | Current |
| 69423-157-73 | 69423015773 | 1 CANISTER in 1 CARTON (69423-157-73) > 73 g in 1 CANISTER | 1 canister | 2016-02-02 | 0000-00-00 | No | No | Current |