Gomina Hand Sanitizer

Gomina Hand Sanitizer
SPL v3
SPL
SPL Set ID a82495fb-2194-b21c-e053-2a95a90acccf
Route
TOPICAL
Published
Effective Date 2020-09-27
Document Type 34390-5 HUMAN OTC DRUG LABEL

Drug Facts

Composition & Product

Active Ingredients
Alcohol (70 mL)
Inactive Ingredients
Fd&c Blue No. 2 Fd&c Yellow No. 5 Fd&c Yellow No. 6 Fd&c Blue No. 1 Glycerin Water Trolamine Carbomer 940 Benzyl Alcohol Methylchloroisothiazolinone/methylisothiazolinone Mixture

Identifiers & Packaging

Pill Appearance
Color: green Color: blue
Marketing Status
OTC MONOGRAPH NOT FINAL Active Since 2020-09-27
Description

Ethyl Alcohol 70% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

Medication Information

Purpose

Antiseptic, Hand Sanitizer

Description

Ethyl Alcohol 70% v/v. Purpose: Antiseptic

Use

Hand Sanitizer to help to decrease bacteria on the skin that could cause disease. Recommended for repeted use.

Section 50565-1

Keep out of reach of children if swallowed, get medical help or contact a Poisson Control Center immediately.

Section 50566-9

Stop use and ask a doctor if irritation or rash appears and lasts.

Section 50567-7

Keep out of eyes, in case of contact, flush thoroughly with water. Avoid contact with broken skin. Do not inhale nor ingest.

Section 53413-1

Questions? +52 444 823 5650

Warnings

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

Directions
  • Put enough product in hands to cover them, rub them together briskly until dry.
  • Children under 6 years old need adult supervision to use this product.
Other Information
  • Store in a cool, dry place at a temperature from 32°F to 95°F.
Label Ndc 79008 001

1000 mL NDC: 79008-001-01

Active Ingredient(s)

Ethyl Alcohol 70% v/v. Purpose: Antiseptic

Inactive Ingredients

carbomer, demineralized water, glycerin, Microcare®CB (benzyl alcohol and a mixture of methylchloroisothiazolinone and methylisothiazolinone) and triethanolamine. May contain FD&C Blue No. 1, FD&C Blue No. 2, FD&C Yellow No. 5 (tartrazine) and/or FD&C Yellow No. 6.

Label Ndc 79008 001 03

1000 mL NDC: 79008-001-03

Bottle w/dispenser

Label Ndc 79008 002 01

1000 mL NDC: 79008-002-01

Label Ndc 79008 002 03

1000 mL NDC: 79008-002-03

Bottle w/dispenser

Label Ndc 79008 003 01

1000 mL NDC: 79008-003-01

Label Ndc 79008 003 03

1000 mL NDC: 79008-003-03

Bottle w/dispenser

Label Ndc: 79008 001 02

220 mL NDC: 79008-001-02

Label Ndc: 79008 002 02

220 mL NDC: 79008-002-02

Label Ndc: 79008 003 02

220 mL NDC: 79008-003-02

Structured Label Content

Use

Hand Sanitizer to help to decrease bacteria on the skin that could cause disease. Recommended for repeted use.

Section 50565-1 (50565-1)

Keep out of reach of children if swallowed, get medical help or contact a Poisson Control Center immediately.

Section 50566-9 (50566-9)

Stop use and ask a doctor if irritation or rash appears and lasts.

Section 50567-7 (50567-7)

Keep out of eyes, in case of contact, flush thoroughly with water. Avoid contact with broken skin. Do not inhale nor ingest.

Section 53413-1 (53413-1)

Questions? +52 444 823 5650

Purpose

Antiseptic, Hand Sanitizer

Warnings

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

Directions
  • Put enough product in hands to cover them, rub them together briskly until dry.
  • Children under 6 years old need adult supervision to use this product.
Other Information (Other information)
  • Store in a cool, dry place at a temperature from 32°F to 95°F.
Label Ndc 79008 001 (Label NDC 79008-001)

1000 mL NDC: 79008-001-01

Active Ingredient(s)

Ethyl Alcohol 70% v/v. Purpose: Antiseptic

Inactive Ingredients (Inactive ingredients)

carbomer, demineralized water, glycerin, Microcare®CB (benzyl alcohol and a mixture of methylchloroisothiazolinone and methylisothiazolinone) and triethanolamine. May contain FD&C Blue No. 1, FD&C Blue No. 2, FD&C Yellow No. 5 (tartrazine) and/or FD&C Yellow No. 6.

Label Ndc 79008 001 03 (Label NDC 79008-001-03)

1000 mL NDC: 79008-001-03

Bottle w/dispenser

Label Ndc 79008 002 01 (Label NDC 79008-002-01)

1000 mL NDC: 79008-002-01

Label Ndc 79008 002 03 (Label NDC 79008-002-03)

1000 mL NDC: 79008-002-03

Bottle w/dispenser

Label Ndc 79008 003 01 (Label NDC 79008-003-01)

1000 mL NDC: 79008-003-01

Label Ndc 79008 003 03 (Label NDC 79008-003-03)

1000 mL NDC: 79008-003-03

Bottle w/dispenser

Label Ndc: 79008 001 02 (Label NDC: 79008-001-02)

220 mL NDC: 79008-001-02

Label Ndc: 79008 002 02 (Label NDC: 79008-002-02)

220 mL NDC: 79008-002-02

Label Ndc: 79008 003 02 (Label NDC: 79008-003-02)

220 mL NDC: 79008-003-02

Advanced Ingredient Data

Raw Label Data

All Sections (JSON)

Additional Information

Back to search View SPL set listing Open on DailyMed ↗

Source: dailymed · Ingested: 2026-02-15T11:58:50.689741 · Updated: 2026-03-14T22:58:38.353182