Aluminum Acetate Astringent
- Product NDC
- 51224-153
- 11-digit product format
- 512240153
- Labeler code
- 51224
- Product ID
- 51224-153_a4b9d3a3-fe12-4313-922f-abc93f440e6c
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Calcium Acetate and Aluminum sulfate
- Dosage form
- POWDER, FOR SOLUTION
- Route
- TOPICAL
- Labeler
- TAGI Pharma Incorporated
- Application
- part347
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2011-06-15
- Marketing end
- 0000-00-00
- Substance
- CALCIUM ACETATE; ALUMINUM SULFATE
- Active strength
- 839 mg/2030mg; mg/2030mg
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51224-153-24 | 51224015324 | 12 BOX in 1 CARTON (51224-153-24) > 12 POUCH in 1 BOX (51224-153-12) > 2030 mg in 1 POUCH (51224-153-99) | 12 box | 2011-06-15 | 0000-00-00 | No | No | Current |