FDA.reportPublic FDA data

NDC 63561-0178-1 - 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
63561-0178
Requested NDC
63561-0178-1
Package NDCs from labels
63561-0178-1, 63561-0178-2
Manufacturer
Granulation Technology, Inc.
Effective date
2025-06-12
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Astringent SolutionGranulation Technology, Inc.2025-06-12HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63561-0178-22025-02-21C16284748780-12cef2736-5d12-d83d-e063-dadaa90ab31fAstringent Solution
63561-0178-22025-01-30C16284748780-12cef2736-5d12-d83d-e063-dadaa90ab31fAstringent Solution

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63561-0178-1Astringent2299 mg in 1 PACKETPOWDER, FOR SOLUTION22993
63561-0178-2Astringent12 in 1 CARTONPOWDER, FOR SOLUTION123

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63561-0178ASTRINGENT (CALCIUM ACETATE MONOHYDRATE AND ALUMINUM SULFATE TETRADECAHYDRATE) POWDER, FOR SOLUTION [GRANULATION TECHNOLOGY, INC.]2Current NDC, 2 package rows20250223_1c2bf19c-2f32-4a22-a371-16cc744dce76.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 1 of 1 ยท 5 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
rxcui: 1250234
unii: E3UT66504P
unii: 7ZA48GIM5H
Astringent SolutionALUMINUM SULFATE TETRADECAHYDRATE, CALCIUM ACETATE MONOHYDRATEFirst Nation Group065c895c-7d86-f1ed-e063-6394a90a3a522025-07-07WarningsExact identifier
rxcui: 1250234
unii: E3UT66504P
unii: 7ZA48GIM5H
AstringentCALCIUM ACETATE MONOHYDRATE AND ALUMINUM SULFATE TETRADECAHYDRATEGranulation Technology, Inc.1c2bf19c-2f32-4a22-a371-16cc744dce762025-06-12WarningsExact identifier
ndc (package): 63561-0178-2
ndc (package): 63561-0178-1
ndc (product): 63561-0178
ndc11 (package): 63561017801
rxcui: 1250234
spl id: 37553cf5-a897-fef9-e063-6394a90a7812
spl set id: 1c2bf19c-2f32-4a22-a371-16cc744dce76
unii: E3UT66504P
unii: 7ZA48GIM5H
Aspartame/MSG DetoxCHELIDONIUM MAJUS, ARNICA MONTANA, PHYTOLACCA DECANDRA, NITRICUM ACIDUM, NUX VOMICA, PHOSPHORICUM ACIDUM, BISPHENOL A (BPA), DEXTROSE, MALTODEXTRIN, SUCRALOSE, ASPARTIC ACID, DIKETOPIPERAZINE, DOPAMINE HYDROCHLORIDE, FORMALINUM, FORMICUM ACIDUM, L-PHENYLALANINE, METHYL ALCOHOL, MONOSODIUM GLUTAMATEDeseret Biologicals, Inc.a1dc1bf3-db71-4550-a975-4f146fb940052025-03-11WarningsExact identifier
unii: 7CVR7L4A2D
DomeboroALUMINUM SULFATE TETRADECAHYDRATE, CALCIUM ACETATE MONOHYDRATEAdvantice Health, LLC.28c39200-2f7c-954b-3ce7-7349b27388122024-12-12WarningsExact identifier
rxcui: 1250234
unii: E3UT66504P
unii: 7ZA48GIM5H

Reported adverse events (FAERS/openFDA)#

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