Benzethonium chloride Plus Dyclonine hydrochloride

Product NDC
69256-037
11-digit product format
692560037
Labeler code
69256
Product ID
69256-037_4094d260-7cad-0cba-e063-6394a90a317d
Type
HUMAN OTC DRUG
Nonproprietary name
Liquid Bandage
Dosage form
LIQUID
Route
TOPICAL
Labeler
Harris Teeter, LLC
Application
M003
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2014-07-10
Substance
BENZETHONIUM CHLORIDE; DYCLONINE HYDROCHLORIDE
Active strength
.2; .75 mg/9mL; 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
Benzethonium chloride Plus Dyclonine hydrochloride
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENZETHONIUM CHLORIDE.2 mg/9mL
DYCLONINE HYDROCHLORIDE.75 mg/9mL

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
69256-037-03Benzethonium chloride Plus Dyclonine hydrochloride9 mL in 1 BOTTLE, WITH APPLICATORLIQUID98

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69256-037BENZETHONIUM CHLORIDE PLUS DYCLONINE HYDROCHLORIDE (LIQUID BANDAGE) LIQUID [HARRIS TEETER, LLC]7Current NDC, Legacy NDC, 1 package rows20241212_15dd2a60-036e-42b3-b68d-2cc1e5eb9746.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69256-037-03692560037039 mL in 1 BOTTLE, WITH APPLICATOR (69256-037-03) 9 ml2014-07-100000-00-00NoNoCurrent