70 Alcohol Hand Sanitizer

Manufacturer: Iron Lab SA de CV
Effective date: 2026-02-17
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 01:46:02

Label at a glance#

Product70 Alcohol Hand Sanitizer

Active ingredientALCOHOL

Label structure11 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Thoroughly cover your hands with product and allow to dry without wiping. Children under 6 years of age should be supervised when using this product. Not recommended for infants.

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin that could cause disease. Recommended for repeated use.

INACTIVE INGREDIENT SECTION

purified water, methyl salicylate, FD&C Blue #1, FD&C Yellow #5

OTC - ACTIVE INGREDIENT SECTION

70% Ethyl Alcohol

WARNINGS SECTION

For external use only: hands. Flammable, Keep away from fire of flame.

OTC - ASK DOCTOR SECTION

Irritation or redness develops. Condition persist for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

OTHER SAFETY INFORMATION

Store below 105°F. May discolor some fabrics. Harmful to wood finishes and plastic

OTC - PURPOSE SECTION

Antiseptic Alcoho

OTC - WHEN USING SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

WinterGreen 70Wintergreen 70

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
582753	ethanol 70 % Topical Solution	PSN	2
582753	ethanol 0.7 ML/ML Topical Solution	SCD	2
582753	ethanol 70 % Topical Solution	SY	2
582753	ethyl alcohol 70 % Topical Solution	SY	2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
74375-060-01	70 Alcohol Hand Sanitizer	355 mL in 1 BOTTLE, PUMP	LIQUID	355		2

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

70 Alcohol Hand Sanitizer
Alcohol
FD&C YELLOW NO. 5
METHYL SALICYLATE
WATER
FD&C BLUE NO. 1

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
74375-060	74375-060-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
FD&C YELLOW NO. 5	I753WB2F1M	IACT
METHYL SALICYLATE	LAV5U5022Y	IACT
WATER	059QF0KO0R	IACT
FD&C BLUE NO. 1	H3R47K3TBD	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
70 Alcohol Hand Sanitizer	ALCOHOL	Iron Lab SA de CV	323c06d5-c984-39b8-e063-6294a90a0d3f	2026-02-17	Warnings	Exact identifier ndc (package): 74375-060-01 ndc (product): 74375-060 ndc11 (package): 74375006001 spl id: 4b08c175-2deb-508a-e063-6294a90a5e1f spl set id: 323c06d5-c984-39b8-e063-6294a90a0d3f

Reported adverse events (FAERS/openFDA)#

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