QuickMend

Product NDC
53228-230
11-digit product format
532280230
Labeler code
53228
Product ID
53228-230_4633776e-e36a-88ee-e063-6294a90aab5b
Type
HUMAN OTC DRUG
Nonproprietary name
BENZETHONIUM CHLORIDE
Dosage form
LIQUID
Route
TOPICAL
Labeler
Equibal, Inc.
Application
M003
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2016-04-01
Substance
BENZETHONIUM CHLORIDE
Active strength
.09 mg/9mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
QuickMend
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENZETHONIUM CHLORIDE.09 mg/9mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiPH41D05744

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829
bb6d6c68-649d-4e6d-a1f6-603d969c8f68Product name120160303

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53228-230-01QuickMend9 mL in 1 CONTAINERLIQUID912
53228-230-02QuickMend4.5 mL in 1 BOTTLE, PUMPLIQUID4.512

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
53228-230-01532280230019 mL in 1 CONTAINER (53228-230-01) 9 ml2016-04-010000-00-00NoNoCurrent
53228-230-02532280230024.5 mL in 1 BOTTLE, PUMP (53228-230-02) 4.5 ml2016-04-010000-00-00NoNoCurrent