Zogics Foam Hand Sanitizer

Product NDC
72202-282
11-digit product format
722020282
Labeler code
72202
Product ID
72202-282_36e8b7a6-4e3c-378e-e063-6394a90a2652
Type
HUMAN OTC DRUG
Nonproprietary name
Benzalakonium
Dosage form
LIQUID
Route
TOPICAL
Labeler
Zogics, LLC
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2017-04-24
Substance
BENZALKONIUM CHLORIDE
Active strength
.12 g/100mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Zogics Foam Hand Sanitizer
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENZALKONIUM CHLORIDE.12 g/100mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiF5UM2KM3W7
Rxcui1046310

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72202-282-00Zogics Foam Hand Sanitizer3785 mL in 1 BOTTLE, PLASTICLIQUID37851

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1046310benzalkonium chloride 0.12 % Topical FoamPSN36e8b7a6-4e3b-378e-e063-6394a90a26521
1046310benzalkonium chloride 1.2 MG/ML Topical FoamSCD36e8b7a6-4e3b-378e-e063-6394a90a26521
1046310benzalkonium chloride 0.12 % Topical FoamSY36e8b7a6-4e3b-378e-e063-6394a90a26521

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
72202-282-00722020282003785 mL in 1 BOTTLE, PLASTIC (72202-282-00) 3785 ml2017-04-24NoNoCurrent