1902 HAND SANITIZER

Manufacturer
Innovation Specialties
Effective date
2023-02-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:36:37

Label at a glance#

Product1902 HAND SANITIZER
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

Spread on both hands, rub in, let dry.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antiseptic

INDICATIONS & USAGE SECTION

Hand sanitizer to help decrease bacteria on the skin.

Warnings

WARNINGS SECTION

Flammable, keep away from fire or flame. For external use only.

When using this product Avoid contact with eyes. In case of contact flush eyes with water.

Stop use and ask a doctor If redness or irritation develop and persist for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children If swallowed get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Spread on both hands, rub in, let dry.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

 Carbomer, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate, Triethanolamine, Water.

Questions?

OTC - QUESTIONS SECTION

Call 1-855-755 5346

SPL UNCLASSIFIED SECTION

Made in China for Innovation Line Culver City, CA 90230
Citrus Scent

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

untitleduntitled

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76138-12276138-122-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Source Document#

Source XML · Source PDF

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
496f2861-8fbb-47ad-9da5-d8e894720e9e5925b83e-c3d4-4b8e-b5d6-7587d466c2b82023-02-14WarningsExact identifier
spl id: 496f2861-8fbb-47ad-9da5-d8e894720e9e
spl set id: 5925b83e-c3d4-4b8e-b5d6-7587d466c2b8

Reported adverse events (FAERS/openFDA)#

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