HANDSANITIZERGELBLOODORANGE- gc-hand sanitizer gel-blood orange gel

HandSanitizerGelBloodOrange by

Drug Labeling and Warnings

HandSanitizerGelBloodOrange by is a Otc medication manufactured, distributed, or labeled by Naturich Labs, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl Alcohol 62%

Purpose

Antiseptic

Uses:

Helps decrease bacteria on skin. Recommended for repeated use

Warnings

Flammable: keep away from fire or flame.

When using this product

- Keep out of eyes

- In case of contact with eyes, flush thoroughly with water.

- Avoid contact with broken skin

Stop Use

Stop use and ask a doctor if irritation or redness develop and persist for more than 72 hours.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center Immediately.

Directions:

Squeeze a small drop onto palms and rub together. For children under 6 years, use adult supervision. Not recommended for infants.

Inactive Ingredients:

Water (Aqua), Propanediol, Aloe Barbadensis (Aloe Vera) Leaf Juice, Caprylic/Capric Triglyceride, Cocos Nucifera (Coconut) Oil, Simmondsia Chinensis (Jojoba) Seed Oil, Helianthus Annuus (Sunflower) Seed Oil, Lavandula Angustifolia (Lavender) Flower Extract, Natural Fragrance*, Aminomethyl Propanol, Carbomer, Citrus Aurantium Bergamia (Bergamo!) Fruit Oil, Tocopheryl Acetate, Citral, Limonene, Linalool.

Other Information:

Store between 16-30C (59-86F).

Avoid freezing and excessive heat above 40C (104F)

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HANDSANITIZERGELBLOODORANGE 
gc-hand sanitizer gel-blood orange gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72496-1130
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	32 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72496-1130-1	59.1 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/21/2020
2	NDC: 72496-1130-2	221.8 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/21/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	01/21/2020

Labeler - Naturich Labs, Inc (124281663)

Registrant - Naturich Labs, Inc (124281663)

Establishment
Name	Address	ID/FEI	Business Operations
Naturich Labs, Inc		124281663	manufacture(72496-1130)