Responsible

Manufacturer
General Printing & Design, Inc.
Effective date
2021-10-07
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:33:58

Label at a glance#

ProductResponsible
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% by volume

Purpose

OTC - PURPOSE SECTION

Antiseptic

INDICATIONS & USAGE SECTION

Uses • For hand washing to decrease bacteria on the skin. • Apply topically to the skin to help prevent cross contamination. • Recommended for repeated use. • Dries in seconds when used as directed.

WARNINGS SECTION

Warnings Flammable, keep away from fire or flame. For external use only. When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. Stop use and ask a doctor if irritation or rash appears and lasts.

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.

DOSAGE & ADMINISTRATION SECTION

Directions • To Open Package: Unscrew lid to remove. Open foil bag. Locate wipe in the center and insert corner of the wipe through opening in lid. DO NOT PUSH FINGER THROUGH OPENING. Replace lip. Pull sheet up slightly to side. Always snap lid cap securely shut between uses to prevent moisture loss. • Use wipe to thoroughly wipe hands, fingers, and wrists. Be sure to use the entire wipe. Allow to dry. • For dirty hands, use first wipe to clean hands, then discard wipe; sanitize with second wipe. • Discard after single use – Do not flush. 

INACTIVE INGREDIENT SECTION

Inactive ingredients Water, Chlorhexidine Diacetate, Benzalkonium Chloride, Nano Silver Ions, Vitamin E

SPL UNCLASSIFIED SECTION

Advanced Moisturizing Formula with Vitamin E

Kills 99.9% of Germs

Distributed by Clover Imaging Group

Hoffman Estates, IL 60169

MADE IN CHINA

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

FDA-Initiated Inactive NDC Indexing#

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76720-01176720-011-01, 76720-011-02, 76720-011-03, 76720-011-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

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
39d77c4d-1055-48f9-b088-1e599bf432ccfa687510-ad08-4ae8-9f47-db6178cb8d442022-07-13WarningsExact identifier
spl set id: fa687510-ad08-4ae8-9f47-db6178cb8d44

Reported adverse events (FAERS/openFDA)#

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