HAND SANITIZER

Manufacturer
Biominerales Pharma, LLC
Effective date
2020-06-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:17:39

Label at a glance#

ProductHAND SANITIZER
Active ingredientAlcohol
Label structure9 sections

Dosage and administration

- Place enough product on hands to cover all surfaces. Rub hands together until dry. - Supervise children under 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

DRUG FACTS

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Inactive ingredients

INACTIVE INGREDIENT SECTION

Carbomer, Glycerin, Propylene Glycol, Aminomethyl Propanol, Isopropyl Myristate, Tocopheryl Acetate, Purified Water, Fragrance.

Use (s)

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when water and soap are not available.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame.

OTC - DO NOT USE SECTION

Do not use in children less than 2 months of age or on open skin wounds.

OTC - WHEN USING SECTION

When using this product keep our of eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact poison control center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

SPL UNCLASSIFIED SECTION

Manufactured for and
Distributed by:

Biominerales Pharma, LLC
Boca Raton, Florida 33442

PRINCIPAL DISPLAY PANEL - 3,785 mL Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BIOMINERALES
PHARMA

HAND SANITIZER - GEL

Kills more than 99.99% of germs

Prevention:
Keep away from heat / sparks / open flames / hot surfaces.
No Smoking. Keep container tightly closed.
Response:
IF IN EYES: Rinse cautiously with water for several minutes.
Remove contact lenses, if present and easy to do. Continue rinsing.
If eye irritation persists: Get medical advice / attention. In case of fire:
Use dry sand, dry chemical or alcohol - resistant foam for extinction.
Storage:
Store in a well-ventilated place. Keep cool. Store Between
15-30 °C (59 - 86 °F). Avoid freezing and excessive heat above
40 °C (104 °F)
Disposal:
Dispose of contents / container to an approved waste disposal plant.

Active Ingredients: Ethyl Alcohol 70% v/v

NDC: 77110-270-01

Manufactured for and
Distributed by:
Biominerales Pharma, LLC
Boca Raton, Florida 33442
www.biomineralespharma.com

Net Contents
1 Gal. (3,785 mL)

PRINCIPAL DISPLAY PANEL - 3,785 mL Bottle Label
PRINCIPAL DISPLAY PANEL - 3,785 mL Bottle Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77110-270-01HAND SANITIZER3785 mL in 1 BOTTLEGEL37851
77110-270-02HAND SANITIZER472 mL in 1 BOTTLEGEL4721
77110-270-03HAND SANITIZER236 mL in 1 BOTTLEGEL2361
77110-270-04HAND SANITIZER118 mL in 1 BOTTLEGEL1181
77110-270-05HAND SANITIZER59 mL in 1 BOTTLEGEL591
77110-270-06HAND SANITIZER944 mL in 1 BOTTLEGEL9441

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77110-270HAND SANITIZER (ALCOHOL) GEL [BIOMINERALES PHARMA, LLC]1Legacy NDC, 6 package rows20200615_5f1b4fa7-4854-4545-bf6c-1826d2af10b2.zip

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
77110-27077110-270-01, 77110-270-06, 77110-270-02, 77110-270-03, 77110-270-04, 77110-270-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
ee42d6e9-30ba-4865-b2ff-144a8b6e02525f1b4fa7-4854-4545-bf6c-1826d2af10b22020-06-11WarningsExact identifier
spl id: ee42d6e9-30ba-4865-b2ff-144a8b6e0252
spl set id: 5f1b4fa7-4854-4545-bf6c-1826d2af10b2

Reported adverse events (FAERS/openFDA)#

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