Hand Sanitizer

Manufacturer
Anthiso Inc. | Anders Wolfgang Rottschafer | Anthiso Inc
Effective date
2020-12-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:35:10

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure10 sections

Indications and uses

Hand Sanitizer that reduces bacteria on the skin including bacteria that may cause disease. Intended for repeated use.

Dosage and administration

Place enough product in your palm to thoroughly cover your hands Rub hands together briskly until dry Children under 6 years of age should be supervised while using this product

Storage and handling

Do not store above 110 °F (43 °C) May discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

This is a hand sanitizer manufactured according to 21 CFR part 210, 211, 333, and 330*.* In Health Care Antiseptic Final Rule: Finalizes rulemaking for healthcare antiseptics, a final monograph determination was not made for three active ingredients: Isopropyl alcohol 70-91.3 percent, Benzalkonium chloride, and Alcohol (ethyl alcohol) 60 to 95 percent. These active ingredients were classified as Category III.

Therefore, according to 21 USC 355h, this hand sanitizer is not required to be the subject of an application approved under section 355 of Title 21 because this hand sanitizer is:

(i) classified in category III for safety or effectiveness in the preamble of a proposed rule establishing a tentative final monograph that is the most recently applicable proposal or determination for such drug issued under part 330 of title 21, Code of Federal Regulations;

(ii) in conformity with-

(I) the conditions of use, including indication and dosage strength, if any, described for the Health care personnel hand rub with the active ingredient Alcohol 60 to 95 percent in such preamble or in an applicable subsequent proposed rule;

(II) the proposed requirements for drugs classified in such tentative final monograph in category I in the most recently proposed rule establishing requirements related to such tentative final monograph and in any final rule establishing requirements that are applicable to the drug; and

(III) the general requirements for nonprescription drugs and conditions or requirements under subsection (b) or (k) of 21 USC 355h; and

(iii) in a dosage form that, immediately prior to March 27, 2020, had been used to a material extent and for a material time under section 321(p)(2) of Title 21.

The hand sanitizer is formulated using only the following ingredients:

Alcohol (ethanol) (USP or Food Chemical Codex (FCC) grade) (71%, volume/volume (v/v)) in an aqueous solution denatured with Isopropanol according to Alcohol and Tobacco Tax and Trade Bureau regulations in 27 CFR part 20.
Aloe Vera Leaf.
AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S)
Sterile distilled water or boiled cold water.

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 71% v/v

Purpose

OTC - PURPOSE SECTION

ANTISEPTIC

Uses

INDICATIONS & USAGE SECTION

Hand Sanitizer that reduces bacteria on the skin including bacteria that may cause disease.

Intended for repeated use.

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame.

For external use only.

OTC - WHEN USING SECTION

When using this product do not use near the eyes.

In case of contact, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

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.

Directions

DOSAGE & ADMINISTRATION SECTION

Place enough product in your palm to thoroughly cover your hands

Rub hands together briskly until dry

Children under 6 years of age should be supervised while using this product

Other information

STORAGE AND HANDLING SECTION

Do not store above 110 °F (43 °C)

May discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Aloe Vera, Isopropyl Alcohol, Sepimax Zen

Questions or comments?

OTC - QUESTIONS SECTION

Call 1-888-691-3008

Monday-Friday 9:00am - 5:00pm

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

These labels are representative of all listed dosage forms:

4oz Front Label4oz Front Label4oz Back Label4oz Back Label

2oz Label2oz Label

12oz Label Reference12oz Label Reference

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81219-341-122022-01-28C16284748780-1d6a99b3a-0087-a426-e053-dadaa90af4c2Anthiso Moisturizing Gel Hand Sanitizer for package sizes: 2oz, 4oz, 8oz, 12oz, 16oz, 1gallon, 5 gallons 55 gallons, 275 gallons.
81219-341-162022-01-28C16284748780-1d6a99b3a-0087-a426-e053-dadaa90af4c2Anthiso Moisturizing Gel Hand Sanitizer for package sizes: 2oz, 4oz, 8oz, 12oz, 16oz, 1gallon, 5 gallons 55 gallons, 275 gallons.
81219-341-202022-01-28C16284748780-1d6a99b3a-0087-a426-e053-dadaa90af4c2Anthiso Moisturizing Gel Hand Sanitizer for package sizes: 2oz, 4oz, 8oz, 12oz, 16oz, 1gallon, 5 gallons 55 gallons, 275 gallons.
81219-341-212022-01-28C16284748780-1d6a99b3a-0087-a426-e053-dadaa90af4c2Anthiso Moisturizing Gel Hand Sanitizer for package sizes: 2oz, 4oz, 8oz, 12oz, 16oz, 1gallon, 5 gallons 55 gallons, 275 gallons.
81219-341-402022-01-28C16284748780-1d6a99b3a-0087-a426-e053-dadaa90af4c2Anthiso Moisturizing Gel Hand Sanitizer for package sizes: 2oz, 4oz, 8oz, 12oz, 16oz, 1gallon, 5 gallons 55 gallons, 275 gallons.
81219-341-412022-01-28C16284748780-1d6a99b3a-0087-a426-e053-dadaa90af4c2Anthiso Moisturizing Gel Hand Sanitizer for package sizes: 2oz, 4oz, 8oz, 12oz, 16oz, 1gallon, 5 gallons 55 gallons, 275 gallons.
81219-341-712022-01-28C16284748780-1d6a99b3a-0087-a426-e053-dadaa90af4c2Anthiso Moisturizing Gel Hand Sanitizer for package sizes: 2oz, 4oz, 8oz, 12oz, 16oz, 1gallon, 5 gallons 55 gallons, 275 gallons.
81219-341-752022-01-28C16284748780-1d6a99b3a-0087-a426-e053-dadaa90af4c2Anthiso Moisturizing Gel Hand Sanitizer for package sizes: 2oz, 4oz, 8oz, 12oz, 16oz, 1gallon, 5 gallons 55 gallons, 275 gallons.
81219-341-802022-01-28C16284748780-1d6a99b3a-0087-a426-e053-dadaa90af4c2Anthiso Moisturizing Gel Hand Sanitizer for package sizes: 2oz, 4oz, 8oz, 12oz, 16oz, 1gallon, 5 gallons 55 gallons, 275 gallons.
81219-341-952022-01-28C16284748780-1d6a99b3a-0087-a426-e053-dadaa90af4c2Anthiso Moisturizing Gel Hand Sanitizer for package sizes: 2oz, 4oz, 8oz, 12oz, 16oz, 1gallon, 5 gallons 55 gallons, 275 gallons.
81219-341-972022-01-28C16284748780-1d6a99b3a-0087-a426-e053-dadaa90af4c2Anthiso Moisturizing Gel Hand Sanitizer for package sizes: 2oz, 4oz, 8oz, 12oz, 16oz, 1gallon, 5 gallons 55 gallons, 275 gallons.

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81219-341-12Hand Sanitizer355 mL in 1 BOTTLE, DISPENSINGGEL3551
81219-341-16Hand Sanitizer473 mL in 1 BOTTLE, DISPENSINGGEL4731
81219-341-20Hand Sanitizer59 mL in 1 BOTTLE, DISPENSINGGEL591
81219-341-21Hand Sanitizer59 mL in 1 BOTTLE, DISPENSINGGEL591
81219-341-40Hand Sanitizer118 mL in 1 BOTTLE, DISPENSINGGEL1181
81219-341-41Hand Sanitizer118 mL in 1 BOTTLE, DISPENSINGGEL1181
81219-341-71Hand Sanitizer3785 mL in 1 JUGGEL37851
81219-341-75Hand Sanitizer18920 mL in 1 PAILGEL189201
81219-341-80Hand Sanitizer236 mL in 1 BOTTLE, DISPENSINGGEL2361
81219-341-95Hand Sanitizer208198 mL in 1 DRUMGEL2081981
81219-341-97Hand Sanitizer1041000 mL in 1 TANKGEL10410001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81219-341HAND SANITIZER (ETHYL ALCOHOL) GEL [ANTHISO INC.]1Legacy NDC, 11 package rows20201215_b54bbc3a-7699-315e-e053-2a95a90a55fa.zip

Products#

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

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

NDC Codes#

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
b54ba9f6-16a4-db59-e053-2995a90ac1fcb54bbc3a-7699-315e-e053-2a95a90a55fa2020-12-02WarningsExact identifier
spl id: b54ba9f6-16a4-db59-e053-2995a90ac1fc
spl set id: b54bbc3a-7699-315e-e053-2a95a90a55fa

Reported adverse events (FAERS/openFDA)#

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