RAIN FOREST HAND SANITIZER- alcohol gel

RAIN FOREST HAND SANITIZER by

Drug Labeling and Warnings

RAIN FOREST HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by Antrix Distribution LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredients

Alcohol 70% v/v

Purpose

Antiseptic

Uses

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

• On children less than 2 months of age.
• On open skin wounds.

When using this product

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

Stop use and ask a doctor if

• Stop use and seek a 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 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 this product to avoid swallowing.

Other information

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

Inactive ingredients

Water, Carbomer, Glycerin, Triethanolamine, Iodopropynyl Butylcarbamate, Methylisothiazolinone.

Questions?

call 888 919 9223

Company Information

DISTRIBUTED BY

Antrix Distribution,

2013 Murcott drive suite E

St. Cloud Fl 34771

Made in Guatemala

Product Packaging - 240 ml

RAIN

FOREST

HAND

SANITIZER

NON STERILE SOLUTION

with moisturizing ingredients

ALCOHOL 70%

BY

NAKED NATURALS

8 fl. oz. / 240ml

INGREDIENTS AND APPEARANCE

RAIN FOREST HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77646-001
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
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77646-001-01	60 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/12/2020
2	NDC: 77646-001-02	120 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/12/2020
3	NDC: 77646-001-03	240 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/12/2020
4	NDC: 77646-001-04	3780 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/12/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/12/2020

Labeler - Antrix Distribution LLC (081436980)