FDA.reportPublic FDA data

Premium Protection Antibacterial Hand

Product NDC
77617-002
11-digit product format
776170002
Labeler code
77617
Product ID
77617-002_b5076cff-1836-4873-b552-ec38eea80c45
Type
HUMAN OTC DRUG
Nonproprietary name
Benzalkonium Chloride
Dosage form
LIQUID
Route
TOPICAL
Labeler
Maintex
Application
M
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2018-04-15
Substance
BENZALKONIUM CHLORIDE
Active strength
13 kg/100kg
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Premium Protection Antibacterial Hand
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENZALKONIUM CHLORIDE13 kg/100kg

Harmonized Identifiers#

Field, Values table
FieldValues
UniiF5UM2KM3W7

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77617-002-01Premium Protection Antibacterial Hand3.80564 kg in 1 BOTTLE, PLASTICLIQUID3.805648
77617-002-02Premium Protection Antibacterial Hand4 in 1 BOXLIQUID48

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77617-002PREMIUM PROTECTION ANTIBACTERIAL HAND (BENZALKONIUM CHLORIDE) LIQUID [MAINTEX]7Current NDC, Legacy NDC, 2 package rows20241215_53bd6860-dde3-4525-ba1b-50f69be09abc.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
77617-002-01776170002013.80564 kg in 1 BOTTLE, PLASTIC3.80564 kgHistorical
77617-002-02776170002024 BOTTLE, PLASTIC in 1 BOX (77617-002-02) / 3.80564 kg in 1 BOTTLE, PLASTIC (77617-002-01) 2018-04-150000-00-00NoNoCurrent