FDA.reportPublic FDA data

SnugZ Hand Sanitizer Gel

Manufacturer
SnugZ/USA, LLC
Effective date
2025-12-29
Label type
HUMAN OTC DRUG LABEL
Version
11
Source
full-release
Hydrated at
2026-06-01 01:29:16

Label at a glance#

ProductSnugZ Hand Sanitizer Gel
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and rub into skin until dry.

WARNINGS SECTION

Warnings: For external use only. Flammable, keep away from fire. Do not use on damaged or broken skin. Keep out of eyes. Rinse with water to remove. Stop use and ask a doctor if rash occurs. Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Aminomethyl Propanol, Carbomer, Water

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Ethyl Alcohol 70% v/v

OTC - PURPOSE SECTION

Purpose: Antiseptic

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

INDICATIONS & USAGE SECTION

Indications: Helps reduce bacteria on skin.

Hand Sanitizer Gel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ZS10-UNSCZS10-UNSC

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN11
581662ethanol 0.7 ML/ML Topical GelSCD11
581662ethanol 70 % Topical GelSY11
581662ethyl alcohol 70 % Topical GelSY11

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76309-301-01SnugZ Hand Sanitizer Gel28 mL in 1 BOTTLEGEL2811
76309-301-02SnugZ Hand Sanitizer Gel56 mL in 1 BOTTLEGEL5611
76309-301-04SnugZ Hand Sanitizer Gel112 mL in 1 BOTTLEGEL11211
76309-301-05SnugZ Hand Sanitizer Gel14 mL in 1 BOTTLEGEL1411
76309-301-08SnugZ Hand Sanitizer Gel224 mL in 1 BOTTLE, PUMPGEL22411
76309-301-19SnugZ Hand Sanitizer Gel56 mL in 1 BOTTLEGEL5611
76309-301-51SnugZ Hand Sanitizer Gel30 mL in 1 TUBEGEL3011
76309-301-61SnugZ Hand Sanitizer Gel39.75 mL in 1 POUCHGEL39.7511
76309-301-62SnugZ Hand Sanitizer Gel85.17 mL in 1 POUCHGEL85.1711
76309-301-81SnugZ Hand Sanitizer Gel28 mL in 1 BOTTLEGEL2811
76309-301-88SnugZ Hand Sanitizer Gel112 mL in 1 POUCHGEL11211
76309-301-91SnugZ Hand Sanitizer Gel28 mL in 1 BOTTLEGEL2811
76309-301-99SnugZ Hand Sanitizer Gel3785.41 mL in 1 JUGGEL3785.4111

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76309-30176309-301-01, 76309-301-02, 76309-301-04, 76309-301-08, 76309-301-19, 76309-301-51, 76309-301-05, 76309-301-81, 76309-301-91, 76309-301-61, 76309-301-62, 76309-301-99, 76309-301-88

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
AMINOMETHYL PROPANEDIOLCZ7BU4QZJZIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
CARBOMER 9404Q93RCW27EIACT

Source Document#

Source XML

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
SnugZ Hand Sanitizer GelHAND SANITIZER GELSnugZ/USA, LLC69bc7a80-0898-4c08-e053-2a91aa0a87a92025-12-29WarningsExact identifier
ndc (package): 76309-301-04
ndc (package): 76309-301-91
ndc (package): 76309-301-01
ndc (package): 76309-301-19
ndc (package): 76309-301-88
ndc (package): 76309-301-02
ndc (package): 76309-301-81
ndc (package): 76309-301-61
ndc (package): 76309-301-99
ndc (package): 76309-301-62
ndc (package): 76309-301-05
ndc (package): 76309-301-08
ndc (package): 76309-301-51
ndc (product): 76309-301
ndc11 (package): 76309030199
ndc11 (package): 76309030102
ndc11 (package): 76309030101
ndc11 (package): 76309030181
ndc11 (package): 76309030119
ndc11 (package): 76309030188
ndc11 (package): 76309030162
ndc11 (package): 76309030105
ndc11 (package): 76309030161
ndc11 (package): 76309030191
ndc11 (package): 76309030108
ndc11 (package): 76309030104
ndc11 (package): 76309030151
spl id: 4720ba94-cc7c-fec5-e063-6394a90a59cb
spl set id: 69bc7a80-0898-4c08-e053-2a91aa0a87a9

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.