Hand Sanitizer

Manufacturer
Bloom Naturals LLC
Effective date
2020-06-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:20:24

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 1-844-333-2133

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 Drug Facts Label4oz Drug Facts Label

4oz Label Front4oz Label Front

12oz Product Label12oz Product Label

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79269-341-10Hand Sanitizer118 mL in 1 BOTTLE, DISPENSINGGEL1181
79269-341-11Hand Sanitizer118 mL in 1 BOTTLE, DISPENSINGGEL1181
79269-341-20Hand Sanitizer236 mL in 1 BOTTLE, DISPENSINGGEL2361
79269-341-30Hand Sanitizer355 mL in 1 BOTTLE, DISPENSINGGEL3551
79269-341-40Hand Sanitizer473 mL in 1 BOTTLE, DISPENSINGGEL4731
79269-341-50Hand Sanitizer3785 mL in 1 BOTTLE, DISPENSINGGEL37851

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79269-341HAND SANITIZER (ETHYL ALCOHOL) GEL [BLOOM NATURALS LLC]1Legacy NDC, 6 package rows20200708_a89b7a62-e646-919b-e053-2a95a90a9e68.zip

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
79269-34179269-341-30, 79269-341-10, 79269-341-50, 79269-341-11, 79269-341-20, 79269-341-40

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
a89b894e-0786-db43-e053-2a95a90a46e9a89b7a62-e646-919b-e053-2a95a90a9e682020-06-27WarningsExact identifier
spl id: a89b894e-0786-db43-e053-2a95a90a46e9
spl set id: a89b7a62-e646-919b-e053-2a95a90a9e68

Reported adverse events (FAERS/openFDA)#

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