Ban
- Product NDC
- 10596-340
- 11-digit product format
- 105960340
- Labeler code
- 10596
- Product ID
- 10596-340_d23058dc-21cc-26e6-e053-2a95a90adeef
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Aluminum Chlorohydrate
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Kao USA Inc.
- Application
- part350
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2012-01-01
- Marketing end
- 0000-00-00
- Substance
- ALUMINUM CHLOROHYDRATE
- Active strength
- 20 g/103mL
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 10596-340 | D | Discontinued by firm | 2026-10-15 | ||
| excluded package | package | 10596-340 | 10596-340-35 | D | Discontinued by firm | 2026-10-15 | |
| excluded package | package | 10596-340 | 10596-340-70 | D | Discontinued by firm | 2026-10-15 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 10596-340-35 | 10596034035 | 103 mL in 1 BOTTLE, WITH APPLICATOR (10596-340-35) | 103 ml | 2012-01-01 | 0000-00-00 | No | No | Current |
| 10596-340-70 | 10596034070 | 2 BOTTLE, WITH APPLICATOR in 1 PACKAGE (10596-340-70) > 103 mL in 1 BOTTLE, WITH APPLICATOR | 2019-12-12 | 0000-00-00 | No | No | Current |