United States · FDA National Drug Code directory
Astringent Solution
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
- 81469-999_395b30e3-c0a9-2267-e063-6294a90aa44b
- Product NDC
- 81469-999
- Form
- POWDER, FOR SOLUTION
- Composition / generic term
- Aluminum Sulfate Tetradecahydrate, Calcium Acetate Monohydrate
- Labeler
- First Nation Group
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20230927
- Source listing expiry
- 20261231
Source-listed ingredients
- CALCIUM ACETATE MONOHYDRATE — 952 mg/2299mg
- ALUMINUM SULFATE TETRADECAHYDRATE — 1347 mg/2299mg
These values do not establish equivalence or a dose recommendation.
Packages
- 12 PACKET in 1 BOX (81469-999-12) / 2299 mg in 1 PACKET (81469-999-01) · 81469-999-12
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 →