Earwax Removal Aid

Product NDC
49762-453
11-digit product format
497620453
Labeler code
49762
Product ID
49762-453_391897b2-7553-4c30-b756-9ac7e7b18e27
Type
HUMAN OTC DRUG
Nonproprietary name
Earwax Removal Aid
Dosage form
LIQUID
Route
AURICULAR (OTIC)
Labeler
Apothecary Products, LLC
Application
part344
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2010-08-31
Marketing end
0000-00-00
Substance
CARBAMIDE PEROXIDE
Active strength
7 mg/100mL
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5eb9f24b-9328-475e-af0a-18021935eb6aProduct name120180220

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
49762-453-152019-11-27C16284748780-19855e2a2-4041-60a7-e053-dbdaa90a05bdEarwax Removal Aid

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49762-453-15Earwax Removal Aid15 mL in 1 BOTTLELIQUID152

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CARBAMIDE PEROXIDEACTIVE INGREDIENT31PZ2VAU81EARWAX REMOVAL AID LIQUID [APOTHECARY PRODUCTS, LLC]2
HYDROGEN PEROXIDEACTIVE MOIETYBBX060AN9VEARWAX REMOVAL AID LIQUID [APOTHECARY PRODUCTS, LLC]2
GLYCERININACTIVE INGREDIENTPDC6A3C0OXEARWAX REMOVAL AID LIQUID [APOTHECARY PRODUCTS, LLC]2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49762-453EARWAX REMOVAL AID LIQUID [APOTHECARY PRODUCTS, LLC]2Legacy NDC, 1 package rows20140527_32bf8ffa-c495-434a-be87-b158998ab379.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
49762-453-154976204531515 mL in 1 BOTTLE15 mlHistorical