REDICARE GEL HAND SANITIZER- gel hand sanitizer gel

Redicare Gel Hand Sanitizer by

Drug Labeling and Warnings

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

Drug Details [pdf]

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 lasts

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

Water, Carbomer, Glycerin, Triethanolamine, Iodopropynyl Butyl Carbamate, Methylisothiazolinone.

PRINCIPAL DISPLAY PANEL

Redicare

GEL HAND SANITIZER

Alcohol Antiseptic 70%

Germ-killing formula

236ml - 8 fl. oz.

Manufactured for

Redicare LLC, Congers, NY

866.561.5650

NDC: 71105-003-08

MADE IN NORTH AMERICA

INGREDIENTS AND APPEARANCE

REDICARE GEL HAND SANITIZER 
gel hand sanitizer gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71105-030
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
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
GLYCERIN (UNII: PDC6A3C0OX)
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71105-030-08	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/18/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/18/2020

Labeler - Redicare LLC (800149346)

Establishment
Name	Address	ID/FEI	Business Operations
Redicare LLC		800149346	relabel(71105-030)