Hand Sanitizer

Manufacturer: INNDEA, S.A. de C.V.
Effective date: 2020-08-05
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:24:24

Label at a glance#

ProductHand 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 age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use(s)

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 mix use with other household chemicals.

Do not use

OTC - DO NOT USE SECTION

- In children less than two months of age.
- On open skin wounds.

When using this product

OTC - WHEN USING SECTION

keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or rash occurs. These maybe signs of serious condititon.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a poision 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 age when using this product to avoid swallowing.

Other information

SPL UNCLASSIFIED SECTION

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Purified water, glicerin, aloe vera extract, tocopheryl acetate (vitamin E).

Questions

OTC - QUESTIONS SECTION

+52 1 55 3775 1431 8:00 AM - 5:00 PM (EAST)

Package Labeling:10ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle

Package Labeling:250ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

250

Package Labeling:500ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

500

Package Labeling:1000ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1

Package Labeling:3780ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

3.78

Package Labeling:1000L

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1000

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
79875-000-01	2022-01-28	C162847	48780-1	d6a99b39-9385-a426-e053-dadaa90af4c2	Hand Sanitizer
79875-000-02	2022-01-28	C162847	48780-1	d6a99b39-9385-a426-e053-dadaa90af4c2	Hand Sanitizer
79875-000-03	2022-01-28	C162847	48780-1	d6a99b39-9385-a426-e053-dadaa90af4c2	Hand Sanitizer
79875-000-04	2022-01-28	C162847	48780-1	d6a99b39-9385-a426-e053-dadaa90af4c2	Hand Sanitizer
79875-000-05	2022-01-28	C162847	48780-1	d6a99b39-9385-a426-e053-dadaa90af4c2	Hand Sanitizer
79875-000-06	2022-01-28	C162847	48780-1	d6a99b39-9385-a426-e053-dadaa90af4c2	Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
79875-000-01	Hand Sanitizer	10 mL in 1 BOTTLE	GEL	10		2
79875-000-02	Hand Sanitizer	250 mL in 1 BOTTLE	GEL	250		2
79875-000-03	Hand Sanitizer	500 mL in 1 BOTTLE	GEL	500		2
79875-000-04	Hand Sanitizer	1000 mL in 1 BOTTLE	GEL	1000		2
79875-000-05	Hand Sanitizer	3780 mL in 1 BOTTLE	GEL	3780		2
79875-000-06	Hand Sanitizer	1000000 mL in 1 BOTTLE	GEL	1000000		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
79875-000	HAND SANITIZER (ALCOHOL) GEL [INNDEA, S.A. DE C.V.]	2	Legacy NDC, 6 package rows	20200812_7fcbd84a-06ba-4f48-a6c2-5a0305c13595.zip

Products#

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

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

Hand Sanitizer
ALCOHOL
WATER
GLYCERIN
ALOE VERA LEAF
.ALPHA.-TOCOPHEROL ACETATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
79875-000	79875-000-01, 79875-000-02, 79875-000-03, 79875-000-04, 79875-000-05, 79875-000-06

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
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
ALCOHOL	3K9958V90M	ACTIB

Source Document#

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
ac222700-e5b4-5f4d-e053-2a95a90ab8e0			7fcbd84a-06ba-4f48-a6c2-5a0305c13595	2020-08-05	Warnings	Exact identifier spl id: ac222700-e5b4-5f4d-e053-2a95a90ab8e0 spl set id: 7fcbd84a-06ba-4f48-a6c2-5a0305c13595

Reported adverse events (FAERS/openFDA)#

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