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Redicare Gentle Touch Gel Hand Sanitizer by

Drug Labeling and Warnings

Redicare Gentle Touch Gel Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Redicare LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

REDICARE GENTLE TOUCH GEL HAND SANITIZER- gel hand sanitizer gel 
Redicare LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Active ingredient

Alcohol 70% v/v

Purpose

Antibacterial Agent

Uses

For personal use for hand sanitizing to decrease bacteria on skin.

Warnings

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

Do not use

• internally
• on face or near eyes - in case of eye contact, flush thoroughly
• near heat/sparks/open flames
• on children less than 2 months old

Ask a doctor if you have

redness or irritation that appears and last

Keep out of reach of children.

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

Directions:

Apply a small amount to palm. Briskly rub, covering hands with product. Allow to dry. Children should always be supervised when using this product.

Inactive ingredients:

Deionized Water, Ceraphyl 31, Glycerin, Hydroxpropylcellulose, Fragrance (Cymbopogon flexuosus; leaves).

Redicare

Gentle touch

GEL HAND SANITIZER

• Alcohol Antiseptic 70%
• High efficacy, germ-killing formula
• Now with lemongrass
• Leaves skin feeling smooth & clean

946ml - 32 fl. oz.

• Paraben Free
• Triclosan Free

Easy on hands, tough on germs.

NDC: 71105-065-32

Manufactured for

Redicare LLC

Congers, NY

866.561.5650

www.redicaredirect.com

MADE IN USA

REDICARE GENTLE TOUCH GEL HAND SANITIZER 
gel hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71105-065
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
LAURYL LACTATE (UNII: G5SU0BFK7O)
GLYCERIN (UNII: PDC6A3C0OX)
HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)
WATER (UNII: 059QF0KO0R)
CYMBOPOGON FLEXUOSUS LEAF (UNII: 7LJ4Y1UJG7)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71105-065-32	946 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/03/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/03/2020	07/01/2021

Labeler - Redicare LLC (800149346)

Revised: 7/2021

Document Id: c62a0bad-815a-433e-e053-2a95a90a5063

34390-5

Set id: a732d149-d6a5-4833-e053-2a95a90a756d

Version: 2

Effective Time: 20210702

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