tazza Alcohol-Free sanitizer

Product NDC
76370-0041
Requested package NDC
76370-0041-0
11-digit product format
763700041
Labeler code
76370
Product ID
76370-0041_52642367-431f-ed1a-e063-6294a90a7fbf
Type
HUMAN OTC DRUG
Nonproprietary name
Benzalkonium Chloride
Dosage form
LIQUID
Route
TOPICAL
Labeler
Tazza Brands East Inc.
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2026-05-20
Substance
BENZALKONIUM CHLORIDE
Active strength
.13 g/.1L
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
tazza Alcohol-Free sanitizer
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENZALKONIUM CHLORIDE.13 g/.1L

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
F5UM2KM3W7Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1049254Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
52642367-431e-ed1a-e063-6294a90a7fbfAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76370-0041-0tazza Alcohol-Free sanitizer1 L in 1 BOTTLELIQUID11

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
tazza Alcohol-Free sanitizerBENZALKONIUM CHLORIDETazza Brands East Inc.52642367-431e-ed1a-e063-6294a90a7fbf2026-05-22WarningsExact identifier
ndc (package): 76370-0041-0
ndc (product): 76370-0041
ndc11 (package): 76370004100

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1049254benzalkonium chloride 0.13 % Topical SolutionPSN52642367-431e-ed1a-e063-6294a90a7fbf1
1049254benzalkonium chloride 1.3 MG/ML Topical SolutionSCD52642367-431e-ed1a-e063-6294a90a7fbf1
1049254benzalkonium chloride 0.13 % Topical SolutionSY52642367-431e-ed1a-e063-6294a90a7fbf1

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1049254benzalkonium chloride 0.13 % Topical SolutionPSN52642367-431e-ed1a-e063-6294a90a7fbf1
1049254benzalkonium chloride 1.3 MG/ML Topical SolutionSCD52642367-431e-ed1a-e063-6294a90a7fbf1
1049254benzalkonium chloride 0.13 % Topical SolutionSY52642367-431e-ed1a-e063-6294a90a7fbf1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
76370-0041-0763700041001 L in 1 BOTTLE (76370-0041-0) 1 l2026-05-20NoNoCurrent