FDA.reportPublic FDA data

Safety First Hand Sanitizer 70% EtOH

Manufacturer
LifeTech Pharma, LLC | LifeTech Pharma
Effective date
2021-01-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:40:07

Label at a glance#

ProductSafety First Hand Sanitizer 70% EtOH
Active ingredientALCOHOL
Label structure15 sections

Indications and uses

Decreases bacteria on skin.

Dosage and administration

• Rub hands thoroughly with product and allow to dry. • For children under 6, use only under adult supervision.

Storage and handling

• Store below 110ºF (43ºC). • May discolor certain fabrics or surfaces.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

This hand Sanitizer was manufactured according to the Federal Register 21 CFR 310, utilizing:

a. USP/FCC grade Ethyl alcohol 99%

b. Distilled/purified water

c. Hydroxypropylcellulose (as Vegetable Cellulose)

d. Glycerin USP/FCC grade

e. Limonene (as fragrance)

f. Aloe Vera extract

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Uses

OTC - WHEN USING SECTION

Decreases bacteria on skin.

Warnings

WARNINGS SECTION

For external use only. Flammable, keep away from flames.

When using this product

INDICATIONS & USAGE SECTION

When using this product keep out of eyes. In case of contact, flush eyes with water.

Stop use

OTC - STOP USE SECTION

Stop use and ask doctor if irritation and redness develop.

Keep out of reach

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• Rub hands thoroughly with product and allow to dry.
• For children under 6, use only under adult supervision.

Other Information

STORAGE AND HANDLING SECTION

• Store below 110ºF (43ºC).
• May discolor certain fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Inactive ingredients Distilled Water,
Vegetable Cellulose,
Glycerin, Aloe Vera, Fragrance.

8 oz Packaging & Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

8 oz label8 oz label8 FL Oz (236 mL) - NDC: 75270-532-08

8 FL OZ (236 mL) NDC: 75270-532-088 FL OZ (236 mL) NDC: 75270-532-08

16 oz Packaging & Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

16 FL Oz ( 473 mL) - NDC: 75270-532-16 16 oz Pump Bottle16 oz Pump Bottle

16 oz label16 oz label

32 oz Packaging & Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

32 FL Oz ( 946 mL) - NDC: 75270-532-32

32 oz bottle32 oz bottle

32 oz label32 oz label

128 oz Packaging & Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1 Gallon (3.78 L) 128 FL Oz - NDC: 75270-105-28

128 oz Pump Bottle128 oz Pump Bottle128 oz Label128 oz 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#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75270-532-082022-07-29C16284748780-1e4f33bdf-a5d3-d8a0-e053-dadaa90a6e4eHand Sanitizer
75270-532-162022-07-29C16284748780-1e4f33bdf-a5d3-d8a0-e053-dadaa90a6e4eHand Sanitizer
75270-532-282022-07-29C16284748780-1e4f33bdf-a5d3-d8a0-e053-dadaa90a6e4eHand Sanitizer
75270-532-322022-07-29C16284748780-1e4f33bdf-a5d3-d8a0-e053-dadaa90a6e4eHand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75270-532-08Safety First Hand Sanitizer 70% EtOH236 mL in 1 BOTTLE, DISPENSINGGEL2361
75270-532-16Safety First Hand Sanitizer 70% EtOH473 mL in 1 BOTTLE, DISPENSINGGEL4731
75270-532-28Safety First Hand Sanitizer 70% EtOH3780 mL in 1 JUGGEL37801
75270-532-32Safety First Hand Sanitizer 70% EtOH946 mL in 1 BOTTLE, DISPENSINGGEL9461

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75270-532SAFETY FIRST HAND SANITIZER 70% ETOH (ETHYL ALCOHOL) GEL [LIFETECH PHARMA, LLC]1Legacy NDC, 4 package rows20210501_c128a74c-78a7-7faa-e053-2a95a90a53ce.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
75270-53275270-532-08, 75270-532-16, 75270-532-32, 75270-532-28

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
ALOE VERA LEAF POLYSACCHARIDESW21O437517IACT
LIMONENE, (+)-GFD7C86Q1WIACT
ALCOHOL3K9958V90MACTIB
HYDROXYPROPYL CELLULOSE, UNSPECIFIED9XZ8H6N6OHIACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT

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
c128a74c-78a8-7faa-e053-2a95a90a53cec128a74c-78a7-7faa-e053-2a95a90a53ce2021-01-01WarningsExact identifier
spl id: c128a74c-78a8-7faa-e053-2a95a90a53ce
spl set id: c128a74c-78a7-7faa-e053-2a95a90a53ce

Reported adverse events (FAERS/openFDA)#

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