United States · FDA National Drug Code directory
Xerac AC
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 0096-0709_44af1725-7f15-9be4-e063-6294a90a3fc8
- Product NDC
- 0096-0709
- Form
- LIQUID
- Composition / generic term
- Xerac AC
- Labeler
- Person and Covey
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 19960601
- Source listing expiry
- 20261231
Source-listed ingredients
- ALUMINUM CHLORIDE — .0625 g/g
These values do not establish equivalence or a dose recommendation.
Packages
- 29.09 g in 1 PACKAGE (0096-0709-35) · 0096-0709-35
- 49.86 g in 1 PACKAGE (0096-0709-60) · 0096-0709-60
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →