FDA.reportPublic FDA data

ShieldForce HS70

Manufacturer
Force Fluids LLC
Effective date
2020-11-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:33:05

Label at a glance#

ProductShieldForce HS70
Active ingredientALCOHOL
Label structure12 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#

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, carbopol, hydroxy ethyl cellulose, fragrance, hydrogen peroxide, purified water USP

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

60 mL NDC: 80743-444-02 HS70 2ozHS70 2oz

118 mL NDC: 80743-444-04 HS70 4ozHS70 4oz

237 mL NDC: 80743-444-08 HS70 8ozHS70 8oz

3785.41 mL NDC: 80743-446-17 HS70 1galHS70 1gal

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#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80743-446-022022-01-28C16284748780-1d6a99b39-cc6f-a426-e053-dadaa90af4c2b361c5a6-b8dd-4062-e053-2995a90a416c
80743-446-042022-01-28C16284748780-1d6a99b39-cc6f-a426-e053-dadaa90af4c2b361c5a6-b8dd-4062-e053-2995a90a416c
80743-446-082022-01-28C16284748780-1d6a99b39-cc6f-a426-e053-dadaa90af4c2b361c5a6-b8dd-4062-e053-2995a90a416c
80743-446-172022-01-28C16284748780-1d6a99b39-cc6f-a426-e053-dadaa90af4c2b361c5a6-b8dd-4062-e053-2995a90a416c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80743-446-02ShieldForce HS7060 mL in 1 BOTTLE, PLASTICGEL601
80743-446-04ShieldForce HS70118 mL in 1 BOTTLE, PLASTICGEL1181
80743-446-08ShieldForce HS70237 mL in 1 BOTTLE, PLASTICGEL2371
80743-446-17ShieldForce HS703785.41 mL in 1 BOTTLE, PLASTICGEL3785.411

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80743-446SHIELDFORCE HS70 (HAND SANITIZER) GEL [FORCE FLUIDS LLC]1Legacy NDC, 4 package rows20201106_b361c5a6-b8dd-4062-e053-2995a90a416c.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80743-44680743-446-02, 80743-446-04, 80743-446-08, 80743-446-17

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
GLYCERINPDC6A3C0OXIACT
FRAGRANCE CLEAN ORC0600327329LCV5BTFIACT
HYDROXYETHYL CELLULOSE, UNSPECIFIEDT4V6TWG28DIACT
HYDROGEN PEROXIDEBBX060AN9VIACT
CARBOMER 9404Q93RCW27EIACT

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
b360d750-5076-135f-e053-2a95a90a3f48b361c5a6-b8dd-4062-e053-2995a90a416c2020-11-05WarningsExact identifier
spl id: b360d750-5076-135f-e053-2a95a90a3f48
spl set id: b361c5a6-b8dd-4062-e053-2995a90a416c

Reported adverse events (FAERS/openFDA)#

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