FDA.reportPublic FDA data

Gel Hand Sanitizer

Manufacturer
Solugen Blending, LLC | Minetta | Slaton
Effective date
2020-11-12
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:33:28

Label at a glance#

ProductGel Hand Sanitizer
Active ingredientALCOHOL
Label structure13 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.

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

This is a hand sanitizer manufactured according to the Temporary Policy for Preparation of Certain Alcohol-Based Hand Sanitizer Products During the Public Health Emergency (CoViD-19); Guidance for Industry.

The hand sanitizer is manufactured using only the following United States Pharmacopoeia (USP) grade ingredients in the preparation of the product (percentage in final product formulation) consistent with World Health Organization (WHO) recommendations:

  1. Alcohol (ethanol) (USP or Food Chemical Codex (FCC) grade) (70%, volume/volume (v/v)) in an aqueous solution denatured according to Alcohol and Tobacco Tax and Trade Bureau regulations in 27 CFR part 20.
  2. Glycerol (0.5% v/v).
  3. Carbomer (0.37% v/v).
  4. Sterile distilled water or boiled cold water.

The firm does not add other active or inactive ingredients. Different or additional ingredients may impact the quality and potency of the product.

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

  • in children less than 2 months of age
  • on open skin wounds

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

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 a 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.

Other information

STORAGE AND HANDLING SECTION

  • Store between 15-30C (59-86F)
  • Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

glycerin, hydrogen peroxide, purified water USP

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

236mL NDC:79975-012-08

236mL NDC:79975-012-08236mL NDC:79975-012-08

3785mL NDC: 79975-012-05

3785 mL NDC: 79975-012-053785 mL NDC: 79975-012-05

18927 mL NDC: 79975-012-04

18927 mL NDC: 79975-012-0418927 mL NDC: 79975-012-04

208197 mL NDC: 79975-012-03

208197 mL NDC: 79975-012-03208197 mL NDC: 79975-012-03

1249186 mL NDC: 79975-012-02

1249186 mL NDC: 79975-012-021249186 mL NDC: 79975-012-02

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN3
581662ethanol 0.7 ML/ML Topical GelSCD3
581662ethanol 70 % Topical GelSY3
581662ethyl alcohol 70 % Topical GelSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79975-012-022022-01-28C16284748780-1d6a99b39-4acb-a426-e053-dadaa90af4c2Gel Hand Sanitizer
79975-012-032022-01-28C16284748780-1d6a99b39-4acb-a426-e053-dadaa90af4c2Gel Hand Sanitizer
79975-012-042022-01-28C16284748780-1d6a99b39-4acb-a426-e053-dadaa90af4c2Gel Hand Sanitizer
79975-012-052022-01-28C16284748780-1d6a99b39-4acb-a426-e053-dadaa90af4c2Gel Hand Sanitizer
79975-012-082022-01-28C16284748780-1d6a99b39-4acb-a426-e053-dadaa90af4c2Gel Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79975-012-02Gel Hand Sanitizer1249186 mL in 1 CONTAINERGEL12491863
79975-012-03Gel Hand Sanitizer208197 mL in 1 DRUMGEL2081973
79975-012-04Gel Hand Sanitizer18927 mL in 1 PAILGEL189273
79975-012-05Gel Hand Sanitizer3785 mL in 1 JUGGEL37853
79975-012-08Gel Hand Sanitizer236 mL in 1 BOTTLEGEL2363

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79975-012GEL HAND SANITIZER GEL [SOLUGEN BLENDING, LLC]3Legacy NDC, 5 package rows20201113_b21c41ba-3a93-ee0e-e053-2a95a90ad96c.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79975-01279975-012-02, 79975-012-03, 79975-012-04, 79975-012-05, 79975-012-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
CARBOMER COPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED)1N11AG4X4LIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
b3ebd102-7e05-2156-e053-2995a90af1f5b21c41ba-3a93-ee0e-e053-2a95a90ad96c2020-11-12WarningsExact identifier
spl id: b3ebd102-7e05-2156-e053-2995a90af1f5
spl set id: b21c41ba-3a93-ee0e-e053-2a95a90ad96c

Reported adverse events (FAERS/openFDA)#

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