FDA.reportPublic FDA data

NDC 15478-005-01 - shing-Releev

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
15478-005
Requested NDC
15478-005-01
Package NDCs from labels
15478-005-01, 15478-005-02
Manufacturer
Topical Pharmaceuticals Inc.
Effective date
2010-11-02
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
DRUGS FACTSTopical Pharmaceuticals Inc.2010-11-02HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
15478-005-022020-02-13C16284748780-1960f7f55-d7c0-8e05-e053-dbdaa90a074aDRUGS FACTS
15478-005-022019-10-29C16284748780-1960f7f55-d7c0-8e05-e053-dbdaa90a074aDRUGS FACTS

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
AllantoinACTIVE INGREDIENT344S277G0ZSHING-RELEEV (BENZALKONIUM CHLORIDE) LIQUID [TOPICAL PHARMACEUTICALS INC.]1
Benzalkonium ChlorideACTIVE INGREDIENTF5UM2KM3W7SHING-RELEEV (BENZALKONIUM CHLORIDE) LIQUID [TOPICAL PHARMACEUTICALS INC.]1
Benzyl AlcoholACTIVE INGREDIENTLKG8494WBHSHING-RELEEV (BENZALKONIUM CHLORIDE) LIQUID [TOPICAL PHARMACEUTICALS INC.]1
AllantoinACTIVE MOIETY344S277G0ZSHING-RELEEV (BENZALKONIUM CHLORIDE) LIQUID [TOPICAL PHARMACEUTICALS INC.]1
BenzalkoniumACTIVE MOIETY7N6JUD5X6YSHING-RELEEV (BENZALKONIUM CHLORIDE) LIQUID [TOPICAL PHARMACEUTICALS INC.]1
Benzyl AlcoholACTIVE MOIETYLKG8494WBHSHING-RELEEV (BENZALKONIUM CHLORIDE) LIQUID [TOPICAL PHARMACEUTICALS INC.]1
Echinacea purpurea flowering topINACTIVE INGREDIENT2EMS3QFX65SHING-RELEEV (BENZALKONIUM CHLORIDE) LIQUID [TOPICAL PHARMACEUTICALS INC.]1
MethylparabenINACTIVE INGREDIENTA2I8C7HI9TSHING-RELEEV (BENZALKONIUM CHLORIDE) LIQUID [TOPICAL PHARMACEUTICALS INC.]1
Potassium SorbateINACTIVE INGREDIENT1VPU26JZZ4SHING-RELEEV (BENZALKONIUM CHLORIDE) LIQUID [TOPICAL PHARMACEUTICALS INC.]1
PropylparabenINACTIVE INGREDIENTZ8IX2SC1OHSHING-RELEEV (BENZALKONIUM CHLORIDE) LIQUID [TOPICAL PHARMACEUTICALS INC.]1
WaterINACTIVE INGREDIENT059QF0KO0RSHING-RELEEV (BENZALKONIUM CHLORIDE) LIQUID [TOPICAL PHARMACEUTICALS INC.]1

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 72 of 72 · 1,426 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Eye WashWATERCVS Pharmacy049cee29-7ec2-4d5b-8308-f522acde43a72017-03-29WarningsExact identifier
unii: 059QF0KO0R
CVS Pain Relieving First Aid AntisepticLIDOCAINE HYDROCHLORIDE, BENZALKONIUM CHLORIDECVS Pharmacy454b1773-eda8-5610-e054-00144ff88e882017-01-04WarningsExact identifier
unii: F5UM2KM3W7
CVS Pharmacy Sensitive Medicated CreamBENZOCAINE, BENZALKONIUM CHLORIDECVS Pharmacy454c3458-7e40-0e5e-e054-00144ff8d46c2017-01-04WarningsExact identifier
unii: F5UM2KM3W7
Sit CleanBENZALKONIUM CHLORIDESit Cleanef2b12f8-89b3-47c4-88bd-8712a84cfc452016-08-18WarningsExact identifier
unii: F5UM2KM3W7
Sterile WaterWATERBaxter Healthcare Company210dc9ab-d6ca-4552-ac19-1be17792d2902016-05-31Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
20dbda91-9eaa-4045-8413-32db362f1644016c9977-9803-4830-be48-222bdc0e24fd2010-11-02WarningsExact identifier
spl id: 20dbda91-9eaa-4045-8413-32db362f1644
spl set id: 016c9977-9803-4830-be48-222bdc0e24fd

Reported adverse events (FAERS/openFDA)#

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