astringent solution

Generic: aluminum sulfate tetradecahydrate, calcium acetate monohydrate

Labeler: first nation group
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name astringent solution
Generic Name aluminum sulfate tetradecahydrate, calcium acetate monohydrate
Labeler first nation group
Dosage Form POWDER, FOR SOLUTION
Routes
TOPICAL
Active Ingredients

aluminum sulfate tetradecahydrate 1347 mg/2299mg, calcium acetate monohydrate 952 mg/2299mg

Manufacturer
First Nation Group

Identifiers & Regulatory

Product NDC 81469-999
Product ID 81469-999_395b30e3-c0a9-2267-e063-6294a90aa44b
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M016
Listing Expiration 2026-12-31
Marketing Start 2023-09-27

Pharmacologic Class

Classes
blood coagulation factor [epc] calcium [cs] cations divalent [cs] increased coagulation factor activity [pe] phosphate binder [epc] phosphate chelating activity [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 81469999
Hyphenated Format 81469-999

Supplemental Identifiers

RxCUI
1250234
UPC
0381469999129
UNII
E3UT66504P 7ZA48GIM5H

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name astringent solution (source: ndc)
Generic Name aluminum sulfate tetradecahydrate, calcium acetate monohydrate (source: ndc)
Application Number M016 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 1347 mg/2299mg
  • 952 mg/2299mg
source: ndc
Packaging
  • 12 PACKET in 1 BOX (81469-999-12) / 2299 mg in 1 PACKET (81469-999-01)
source: ndc

Packages (1)

Ingredients (2)

aluminum sulfate tetradecahydrate (1347 mg/2299mg) calcium acetate monohydrate (952 mg/2299mg)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "395b30e3-c0a9-2267-e063-6294a90aa44b", "openfda": {"upc": ["0381469999129"], "unii": ["E3UT66504P", "7ZA48GIM5H"], "rxcui": ["1250234"], "spl_set_id": ["065c895c-7d86-f1ed-e063-6394a90a3a52"], "manufacturer_name": ["First Nation Group"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 PACKET in 1 BOX (81469-999-12)  / 2299 mg in 1 PACKET (81469-999-01)", "package_ndc": "81469-999-12", "marketing_start_date": "20230927"}], "brand_name": "Astringent Solution", "product_id": "81469-999_395b30e3-c0a9-2267-e063-6294a90aa44b", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["Blood Coagulation Factor [EPC]", "Calcium [CS]", "Cations", "Divalent [CS]", "Increased Coagulation Factor Activity [PE]", "Phosphate Binder [EPC]", "Phosphate Chelating Activity [MoA]"], "product_ndc": "81469-999", "generic_name": "Aluminum Sulfate Tetradecahydrate, Calcium Acetate Monohydrate", "labeler_name": "First Nation Group", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Astringent Solution", "active_ingredients": [{"name": "ALUMINUM SULFATE TETRADECAHYDRATE", "strength": "1347 mg/2299mg"}, {"name": "CALCIUM ACETATE MONOHYDRATE", "strength": "952 mg/2299mg"}], "application_number": "M016", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230927", "listing_expiration_date": "20261231"}