Hands First

Manufacturer
Avadim II LLC
Effective date
2010-07-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:52:39

Label at a glance#

ProductHands First 4 in 1
Active ingredientAllantoin, Benzalkonium Chloride
Label structure2 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Allantoin 0.5%
Benzalkonium Chloride 0.13%

OTC - PURPOSE SECTION

Skin Protectant

Antimicrobial

Use(s)

For handwashing to decrease bacteria on the skin

For temporary protection of minor cuts, scrapes, burns, and chapped or cracked skin

Directions

Use as needed

Remove cap and pump foam into palm of hand.

Rub foam onto hands

Allow to air dry

WARNINGS SECTION

For external use only
Keep out of the reach of children
Do not use in the eyes
Do not use on deep or puncture wounds, animal bites, or serious burns
Extended use may increase risk of sunburn

OTC - STOP USE SECTION

Stop use and ask a doctor if condition worsens or symptoms last more than seven days.

INACTIVE INGREDIENT SECTION

Purified Water, tego-betaine, aloe vera, dimethicone, *collodial silver, glycolic acid, potassium hydroxide, EDTA, phenoxyethanol, isobutyl paraben, propyl paraben, ethyl paraben, butyl paraben, methyl paraben

*Preservative only .1%

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hands First
4 in 1 action
Alcohol Free Foam
Hand Sanitizer
Doctor created and hospital tested
Temporarily  protect minor cuts and scrapes
Sanitize anytime, anywhere
Hydrate your skin
Clean without water

Kills 99.99% of germs
Attack Recontamination
1.7 fl oz (50mL)

MM2
HF2.jpg
image of bottle
image of bottle


FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51098-742-012021-09-08C16284748780-1956f9ecf-d0bf-621f-e053-dbdaa90a74adDrug Facts
51098-742-022021-09-08C16284748780-1956f9ecf-d0bf-621f-e053-dbdaa90a74adDrug Facts
51098-742-012019-10-21C16284748780-1956f9ecf-d0bf-621f-e053-dbdaa90a74adDrug Facts
51098-742-022019-10-21C16284748780-1956f9ecf-d0bf-621f-e053-dbdaa90a74adDrug Facts

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AllantoinACTIVE INGREDIENT344S277G0Z1
Benzalkonium ChlorideACTIVE INGREDIENTF5UM2KM3W71
AllantoinACTIVE MOIETY344S277G0Z1
BenzalkoniumACTIVE MOIETY7N6JUD5X6Y1

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51098-74251098-742-02, 51098-742-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
Allantoin344S277G0ZACTIB
Benzalkonium ChlorideF5UM2KM3W7ACTIB

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
bce834aa-e88d-43b2-9b3f-41235cb0fb9001ea4e77-a5c1-458c-b2d1-9377d19f18c22021-08-31WarningsExact identifier
spl set id: 01ea4e77-a5c1-458c-b2d1-9377d19f18c2

Reported adverse events (FAERS/openFDA)#

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