AMORA HAND SANITIZER COCONUT- alcohol spray

Amora Hand Sanitizer Coconut by

Drug Labeling and Warnings

Amora Hand Sanitizer Coconut by is a Otc medication manufactured, distributed, or labeled by I World LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Ethyl Alcohol 70% v/v

Purpose

Antibacterial

Uses

• For hand-washing to decrease bacteria on the skin.

Warnings

For external use only.

Flammabel, keep away from fire and flames

when using this product

• test on a small area of skin before full use.
• keep out of eyes. In case of contact with eyes, flush throughly with water.
• Avoid contact with broken skin.
• Do not inhale or ingest.

Stop use and ask doctor if

• allergy, irritation or redness develops.
• Condition persists for more than 72 hours.

Keep out of reach of children.

• If product is swallowed, get medical help or contact a poison control centre right away.

Directions

• Spray hands with product and allow to dry without wiping.
• For children under 6, use only under adult supervision.
• Not recommended for infants.

Other information

• Do not store above 105° F
• May discolor some fabrics
• Harmful to wood finishes and plastics

Inactive ingredients

WATER (AQUA), FRAGRANCE (PARFUM), COCOS NUCIFERA COCONUT WATER, BUTYLENE GLYCOL, HYDROXYACETOPHENONE.

Questions or comments?

1-212-244-5170  info@amora.beauty

Package Labeling:

INGREDIENTS AND APPEARANCE

AMORA HAND SANITIZER COCONUT 
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85179-038
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
COCOS NUCIFERA WHOLE (UNII: 245J88W96L)
WATER (UNII: 059QF0KO0R)
COCONUT WATER (UNII: 267F5Y81NT)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85179-038-00	45 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/17/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	11/17/2025

Labeler - I World LLC (830590126)

Registrant - I World LLC (830590126)