FDA.reportPublic FDA data

NDC 51224-162-99 - Astringent

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
51224-162
Requested NDC
51224-162-99
Package NDCs from labels
51224-162-99, 51224-162-12, 51224-162-24
Manufacturer
TAGI Pharma Inc.
Effective date
2023-03-20
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Astringent SolutionTAGI Pharma Inc.2023-03-20HUMAN OTC DRUG LABEL
National Council for Prescription Drug Programs indexing - billing unitNational Council for Prescription Drug Programs2013-02-13Indexing - Billing Unit

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
51224-162-12EA - Each51224-162f11a6c35-8e94-4224-b8bf-4a21034b20e012013-02-13
51224-162-24EA - Each51224-1622216e56f-2b65-492c-b020-93626e23189012013-02-13
51224-162-99EA - Each51224-1623039ad48-006a-439e-91ff-cb78e925903e12013-02-13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
Aluminum sulfate tetradecahydrateACTIVE INGREDIENTE3UT66504PASTRINGENT (CALCIUM ACETATE MONOHYDRATE AND ALUMINUM SULFATE TETRADECAHYDRATE) POWDER, FOR SOLUTION [TAGI PHARMA INC.]2
Calcium acetate monohydrateACTIVE INGREDIENT7ZA48GIM5HASTRINGENT (CALCIUM ACETATE MONOHYDRATE AND ALUMINUM SULFATE TETRADECAHYDRATE) POWDER, FOR SOLUTION [TAGI PHARMA INC.]2
Aluminum CationACTIVE MOIETY3XHB1D032BASTRINGENT (CALCIUM ACETATE MONOHYDRATE AND ALUMINUM SULFATE TETRADECAHYDRATE) POWDER, FOR SOLUTION [TAGI PHARMA INC.]2
Calcium CationACTIVE MOIETY2M83C4R6ZBASTRINGENT (CALCIUM ACETATE MONOHYDRATE AND ALUMINUM SULFATE TETRADECAHYDRATE) POWDER, FOR SOLUTION [TAGI PHARMA INC.]2
icodextrinINACTIVE INGREDIENT2NX48Z0A9GASTRINGENT (CALCIUM ACETATE MONOHYDRATE AND ALUMINUM SULFATE TETRADECAHYDRATE) POWDER, FOR SOLUTION [TAGI PHARMA INC.]2

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 1 of 1 ยท 9 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Kerasal Athletes Foot Rapid Symptom Relief Medicated SoakALUMINUM SULFATE TETRADECAHYDRATE AND CALCIUM ACETATE MONOHYDRATEAdvantice Health, LLC.09a178c1-0eb1-43e5-bde8-fd27ed633d592026-01-26WarningsExact identifier
unii: E3UT66504P
unii: 7ZA48GIM5H
Astringent SolutionALUMINUM SULFATE TETRADECAHYDRATE, CALCIUM ACETATE MONOHYDRATEFirst Nation Group065c895c-7d86-f1ed-e063-6394a90a3a522025-07-07WarningsExact identifier
unii: E3UT66504P
unii: 7ZA48GIM5H
EXTRANEALICODEXTRIN, SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDEVantive US Healthcare LLCd5b85158-b0d6-4855-9d07-8d1b3ad9ab712025-06-30Warnings, Adverse reactionsExact identifier
unii: 2NX48Z0A9G
AstringentCALCIUM ACETATE MONOHYDRATE AND ALUMINUM SULFATE TETRADECAHYDRATEGranulation Technology, Inc.1c2bf19c-2f32-4a22-a371-16cc744dce762025-06-12WarningsExact identifier
unii: E3UT66504P
unii: 7ZA48GIM5H
EXTRANEALICODEXTRIN, SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDEVantive US Healthcare LLC5bf31b49-24c8-4021-98da-33a151f2fcbe2025-05-08Exact identifier
unii: 2NX48Z0A9G
EXTRANEALICODEXTRIN, SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDEVantive US Healthcare LLCe18bacfe-af60-49dc-bd30-cb3c29fa16db2025-05-07Exact identifier
unii: 2NX48Z0A9G
EXTRANEALICODEXTRIN, SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDEVantive US Healthcare LLC2b327b13-a0e9-4b2c-9875-4470998e2e302025-05-07Exact identifier
unii: 2NX48Z0A9G
DomeboroALUMINUM SULFATE TETRADECAHYDRATE, CALCIUM ACETATE MONOHYDRATEAdvantice Health, LLC.28c39200-2f7c-954b-3ce7-7349b27388122024-12-12WarningsExact identifier
unii: E3UT66504P
unii: 7ZA48GIM5H
4056d8c0-ca3f-4f8c-9fee-af9727a6526745c351e9-5046-496e-9812-5b8b9abcd4ad2023-03-20WarningsExact identifier
spl id: 4056d8c0-ca3f-4f8c-9fee-af9727a65267
spl set id: 45c351e9-5046-496e-9812-5b8b9abcd4ad

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.