Home NDC 81469-999 Astringent Solution
Product NDC 81469-999
11-digit product format 814690999
Labeler code 81469
Product ID 81469-999_395b30e3-c0a9-2267-e063-6294a90aa44b
Type HUMAN OTC DRUG
Nonproprietary name Aluminum Sulfate Tetradecahydrate, Calcium Acetate Monohydrate
Dosage form POWDER, FOR SOLUTION
Route TOPICAL
Labeler First Nation Group
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-09-27
Substance CALCIUM ACETATE MONOHYDRATE; ALUMINUM SULFATE TETRADECAHYDRATE
Active strength 952; 1347 mg/2299mg; mg/2299mg
Pharmacologic classes Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-01-11 03:41 UTC · source 2025-01-10 excluded product product 81469-999 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 81469-999 81469-999-12 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Astringent Solution
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CALCIUM ACETATE MONOHYDRATE 952 mg/2299mg ALUMINUM SULFATE TETRADECAHYDRATE 1347 mg/2299mg
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 7ZA48GIM5H Internal UNII lookup E3UT66504P Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1250234 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 81469-999-01 Astringent Solution 2299 mg in 1 PACKET POWDER, FOR SOLUTION 2299 5 81469-999-12 Astringent Solution 12 in 1 BOX POWDER, FOR SOLUTION 12 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 81469-999 ASTRINGENT SOLUTION (ALUMINUM SULFATE TETRADECAHYDRATE, CALCIUM ACETATE MONOHYDRATE) POWDER, FOR SOLUTION [FIRST NATION GROUP] 4 Current NDC, 2 package rows 20250305_065c895c-7d86-f1ed-e063-6394a90a3a52.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 6 of 68 · 1,350 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 81469-999-01 81469099901 2299 mg in 1 PACKET 2299 mg Historical 81469-999-12 81469099912 12 PACKET in 1 BOX (81469-999-12) / 2299 mg in 1 PACKET (81469-999-01) 12 packet 2023-09-27 No No Current