CERTAIN DRI
- Product NDC
- 0295-0122
- 11-digit product format
- 002950122
- Labeler code
- 0295
- Product ID
- 0295-0122_4037c417-3442-4316-b3b1-63a4dbc27385
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aluminum Chloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Denison Pharmaceuticals, LLC.
- Application
- part350
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2017-01-01
- Marketing end
- 0000-00-00
- Substance
- ALUMINUM CHLORIDE
- Active strength
- 0 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0295-0122-07 | 00295012207 | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (0295-0122-07) > 35.5 mL in 1 BOTTLE, WITH APPLICATOR | 2017-01-01 | 0000-00-00 | No | No | Current |
| 0295-0122-12 | 00295012212 | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (0295-0122-12) > 59.15 mL in 1 BOTTLE, WITH APPLICATOR | 2017-01-01 | 0000-00-00 | No | No | Current |