GC HAND SANITIZER GEL LAVENDER- hand sanitizer gel

GC Hand Sanitizer Gel Lavender by

Drug Labeling and Warnings

GC Hand Sanitizer Gel Lavender by is a Otc medication manufactured, distributed, or labeled by Naturich Labs. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Alcohol 65% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

Use

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

For external use only. Flammable. Keep away from heat or flame.

Do not use

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

WHEN USING

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water. Stop use and ask doctor if irritation or rash occurs. These may be signs of a serious condition. Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away.

STOP USE

Stop use and ask doctor if irritation or rash occurs. These may be signs of a serious condition.

KEEP OUT OF REACH OF CHILDREN

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

Directions

Place enough product on hands to cover all surfaces. Rub hands together until dry.
Supervise children under 6 years of age when using product to avoid swallowing.

Other Information

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

Inactive Ingredients

Aloe Barbadensis Leaf Juice, Aminomethyl Propanol, Camellia Sinensis Leaf Extract, Caprylic/Capric Triglyceride, Carbomer, Carthamus Tinctorius (Safflower) Seed Oil, Fragrance, Geranium Maculatum Extract, Glycerin, Lavandula Angustifolia (Lavender) Flower Extract, Propanediol, Tocopheryl Acetate, Water (Aqua).

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GC HAND SANITIZER GEL LAVENDER 
hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72496-1117
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	65 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	35 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72496-1117-1	60 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/01/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/01/2021

Labeler - Naturich Labs (124281663)

Registrant - Naturich Labs (124281663)

Establishment
Name	Address	ID/FEI	Business Operations
Naturich Labs		124281663	manufacture(72496-1117)