Benzethonium Chloride and Dyclonine Hydrochloride

Product NDC
69842-084
11-digit product format
698420084
Labeler code
69842
Product ID
69842-084_4093b87e-658d-5c45-e063-6294a90a9692
Type
HUMAN OTC DRUG
Nonproprietary name
Liquid Bandage
Dosage form
LIQUID
Route
TOPICAL
Labeler
CVS Pharmacy
Application
M003
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2019-06-01
Substance
BENZETHONIUM CHLORIDE; DYCLONINE HYDROCHLORIDE
Active strength
.2; .75 mg/10mL; mg/10mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Benzethonium Chloride and Dyclonine Hydrochloride
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENZETHONIUM CHLORIDE.2 mg/10mL
DYCLONINE HYDROCHLORIDE.75 mg/10mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiPH41D05744, ZEC193879Q

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
1da7d10e-498b-41dd-970f-0f5bd7432f39Product name120190228

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69842-084-30Benzethonium Chloride and Dyclonine Hydrochloride10 mL in 1 BOTTLE, WITH APPLICATORLIQUID107

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69842-084BENZETHONIUM CHLORIDE AND DYCLONINE HYDROCHLORIDE (LIQUID BANDAGE) LIQUID [CVS PHARMACY]6Current NDC, Legacy NDC, 1 package rows20241116_83ec5d77-3179-0fd6-e053-2a91aa0ace1b.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69842-084-306984200843010 mL in 1 BOTTLE, WITH APPLICATOR (69842-084-30) 10 ml2019-06-010000-00-00NoNoCurrent