Xerac AC
- Product NDC
- 0096-0709
- 11-digit product format
- 000960709
- Labeler code
- 0096
- Product ID
- 0096-0709_44af1725-7f15-9be4-e063-6294a90a3fc8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Xerac AC
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Person and Covey
- Application
- M019
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 1996-06-01
- Substance
- ALUMINUM CHLORIDE
- Active strength
- .0625 g/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Xerac AC
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ALUMINUM CHLORIDE | .0625 g/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3CYT62D3GA |
| Rxcui | 197324 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0096-0709-35 | Xerac AC | 29.09 g in 1 PACKAGE | LIQUID | 29.09 | | 14 |
| 0096-0709-60 | Xerac AC | 49.86 g in 1 PACKAGE | LIQUID | 49.86 | | 14 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0096-0709 | XERAC AC LIQUID [PERSON AND COVEY] | 12 | Current NDC, Legacy NDC, 2 package rows | 20240102_59e37deb-01da-465f-b806-ff1a76255e71.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0096-0709-35 | 00096070935 | 29.09 g in 1 PACKAGE (0096-0709-35) | 29.09 g | 1996-06-01 | 0000-00-00 | No | No | Current |
| 0096-0709-60 | 00096070960 | 49.86 g in 1 PACKAGE (0096-0709-60) | 49.86 g | 1996-06-01 | 0000-00-00 | No | No | Current |