FDA.reportPublic FDA data

Biomax USA HAND SANITIZER

Manufacturer
Biomax Cosmetics
Effective date
2020-07-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:23:13

Label at a glance#

ProductBiomax USA HAND SANITIZER
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

For hand washing to help reduce bacteria on the skin.

Dosage and administration

• Put a small amount in your palm and rub hands together until dry. • Children under 6 years of age should be supervised when using this product. Recommended for repeated use.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Water(Aqua), SDA Alcohol, Triethanolamine, Carbomer, Aloe Barbadensis, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate (Vitamin E), CI 42090, CI 19140.

Uses:

INDICATIONS & USAGE SECTION

For hand washing to help reduce bacteria on the skin.

Directions

DOSAGE & ADMINISTRATION SECTION

• Put a small amount in your palm and rub hands together until dry.

• Children under 6 years of age should be supervised when using this product. Recommended for repeated use.

Warnings

WARNINGS SECTION

For external use only-hands.

Flammable. Keep away from heat and flame.

Stop use and ask a doctor if irritation or redness develops and lasts.

When using this product

• Keep out of eyes. In case of contact with eyes, flush thoroughly with water.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If Swallowed, get medical help or contact a Poison Control Center immediately.

SPL UNCLASSIFIED SECTION

ADVANCED Hand Sanitizer

MOISTURIZING WITH VITAMIN E & ALOE

KILLS 99.99% OF MOST GERMS

MADE IN USA

Manufactured by:

Biomax Cosmetics Inc.

Houston, TX 77061

www.biomaxcosmetics.com

BENEFITS:

• With Vitamin E.

• Leaves hands feeling soft & refreshed.

• Kills more than 99.99% of germs and bacteria.

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagingPackaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN1
582753ethanol 0.7 ML/ML Topical SolutionSCD1
582753ethanol 70 % Topical SolutionSY1
582753ethyl alcohol 70 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77369-927-012022-01-28C16284748780-1d6a99b39-7852-a426-e053-dadaa90af4c2Biomax ADVANCED Hand Sanitizer
77369-927-022022-01-28C16284748780-1d6a99b39-7852-a426-e053-dadaa90af4c2Biomax ADVANCED Hand Sanitizer
77369-927-062022-01-28C16284748780-1d6a99b39-7852-a426-e053-dadaa90af4c2Biomax ADVANCED Hand Sanitizer
77369-927-082022-01-28C16284748780-1d6a99b39-7852-a426-e053-dadaa90af4c2Biomax ADVANCED Hand Sanitizer
77369-927-162022-01-28C16284748780-1d6a99b39-7852-a426-e053-dadaa90af4c2Biomax ADVANCED Hand Sanitizer
77369-927-322022-01-28C16284748780-1d6a99b39-7852-a426-e053-dadaa90af4c2Biomax ADVANCED Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77369-927-01Biomax USA HAND SANITIZER3785 mL in 1 JUGLIQUID37851
77369-927-02Biomax USA HAND SANITIZER59 mL in 1 BOTTLELIQUID591
77369-927-06Biomax USA HAND SANITIZER177 mL in 1 BOTTLELIQUID1771
77369-927-08Biomax USA HAND SANITIZER236.6 mL in 1 BOTTLELIQUID236.61
77369-927-16Biomax USA HAND SANITIZER473 mL in 1 BOTTLELIQUID4731
77369-927-32Biomax USA HAND SANITIZER946 mL in 1 BOTTLELIQUID9461

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77369-927BIOMAX USA HAND SANITIZER (ETHYL ALCOHOL) LIQUID [BIOMAX COSMETICS]1Legacy NDC, 6 package rows20200731_326ba815-c498-4899-baba-ae0b20975c52.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77369-92777369-927-02, 77369-927-06, 77369-927-08, 77369-927-16, 77369-927-32, 77369-927-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
TROLAMINE9O3K93S3TKIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
ALOEV5VD430YW9IACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
FD&C BLUE NO. 1H3R47K3TBDIACT
FD&C YELLOW NO. 5I753WB2F1MIACT

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
4049672d-f14e-42e0-a518-1a70018dbbc9326ba815-c498-4899-baba-ae0b20975c522020-07-27WarningsExact identifier
spl id: 4049672d-f14e-42e0-a518-1a70018dbbc9
spl set id: 326ba815-c498-4899-baba-ae0b20975c52

Reported adverse events (FAERS/openFDA)#

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