FDA.reportPublic FDA data

Hand Sanitizing Gel

Manufacturer
Forward Science Technologies LLC
Effective date
2020-10-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:31:05

Label at a glance#

ProductHand Sanitizing Gel
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

Wet hands thouroughly with product and allow to dry without wiping. For children under 6, use only under adult supervision.

Storage and handling

Do not store above 105ºF May discolor some fabrics Harmful to wood finishes and plastics

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v

Do Not Use

OTC - DO NOT USE SECTION

  • In children less than 2 months of age
  • On open skin wounds

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Purpose

OTC - PURPOSE SECTION

Antiseptic

Stop use and ask a doctor

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • irritation or redness develops
  • condition persists for more than 72 hours

When using this product

OTC - WHEN USING SECTION

keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid with contact with broken skin. Do not inhale or ingest.

Warnings

WARNINGS SECTION

For external use only: hands. Flammable, keep away from fire or flame.

Other information

STORAGE AND HANDLING SECTION

Do not store above 105ºF

May discolor some fabrics

Harmful to wood finishes and plastics

Use(s)

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin that coould cuase disease. Recommended for repeated use.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thouroughly with product and allow to dry without wiping.

For children under 6, use only under adult supervision.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Fragrance, Glycerin, Isopropyl Myristate, Polyethylene Glycol/Acrylates Copolymer, Tocopheryl Acetate, Water

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

16ozGelLabel16ozGelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN2
581662ethanol 0.7 ML/ML Topical GelSCD2
581662ethanol 70 % Topical GelSY2
581662ethyl alcohol 70 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70275-124-012022-01-28C16284748780-1d6a99b39-b140-a426-e053-dadaa90af4c2Hand Sanitizer
70275-124-042022-01-28C16284748780-1d6a99b39-b140-a426-e053-dadaa90af4c2Hand Sanitizer
70275-124-162022-01-28C16284748780-1d6a99b39-b140-a426-e053-dadaa90af4c2Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70275-124-01Hand Sanitizing Gel3790 mL in 1 BOTTLEGEL37902
70275-124-04Hand Sanitizing Gel118 mL in 1 BOTTLE, DISPENSINGGEL1182
70275-124-16Hand Sanitizing Gel473 mL in 1 BOTTLE, PUMPGEL4732

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70275-124HAND SANITIZING GEL (HAND SANITIZER) GEL [FORWARD SCIENCE TECHNOLOGIES LLC]2Legacy NDC, 3 package rows20201007_ae70b13e-e2d5-41ee-e053-2a95a90a1d92.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
70275-12470275-124-16, 70275-124-04, 70275-124-01

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
RAPIDGEL EZ133JH4A7R2KIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
.ALPHA.-TOCOPHEROL ACETATE, DL-WR1WPI7EW8IACT
GLYCERINPDC6A3C0OXIACT
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
b106cea8-1be8-4ce7-e053-2a95a90ac57dae70b13e-e2d5-41ee-e053-2a95a90a1d922020-10-06WarningsExact identifier
spl id: b106cea8-1be8-4ce7-e053-2a95a90ac57d
spl set id: ae70b13e-e2d5-41ee-e053-2a95a90a1d92

Reported adverse events (FAERS/openFDA)#

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