NDC 81636-002-01 - Alcohol Prep Pads Medium

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
81636-002
Requested NDC
81636-002-01
Package NDCs from labels
81636-002-01, 81636-002-02
Manufacturer
Zhejiang Xingheng medical supplies Co., Ltd
Effective date
2021-12-02
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Alcohol Prep Pads Medium - Zhejiang Xingheng medical supplies Co., LtdZhejiang Xingheng medical supplies Co., Ltd2021-12-02HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81636-002-022023-01-30C16284748780-1f386c649-b4db-0266-e053-dadaa90a7c1ad1955408-63be-3ad9-e053-2a95a90aa213

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 40 of 40 · 785 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Bio Rock WaterROCK WATERBioActive Nutritional, Inc.178bd16d-0d4f-49d8-866b-8ab3a3c6889d2018-07-30WarningsExact identifier
unii: 059QF0KO0R
ENT Essentials All Dry Ear Drying DropsISOPROPYL ALCOHOLWisconsin Pharmacal Company5f0bb412-577e-3155-e053-2a91aa0a7f532017-11-28WarningsExact identifier
unii: ND2M416302
Sterile WaterWATERBaxter Healthcare Corporationef3e79c5-3f58-4b36-a296-64b7d9a651c12017-10-17Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Eye WashWATERCVS Pharmacy049cee29-7ec2-4d5b-8308-f522acde43a72017-03-29WarningsExact identifier
unii: 059QF0KO0R
Sterile WaterWATERBaxter Healthcare Company210dc9ab-d6ca-4552-ac19-1be17792d2902016-05-31Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R

Reported adverse events (FAERS/openFDA)#

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