CARE PLUS HAND SANITIZER- ethyl alcohol gel

Care Plus Hand Sanitizer by

Drug Labeling and Warnings

Care Plus Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Ostl, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Ethyl Alcohol 70.0% v/v

Purpose

Antimicrobial

INDICATIONS & USAGE

Uses hand sanitizer to help reduce bacteria on the skin.

Warnings

For external use only.

Flammable. Keep away from heat and flame.

When using this product avoid contact with face, eyes, and broken skin. In case of eye contact, flush with plenty of water and seek medical advice.

Stop use and ask a doctor if irritation or redness develops.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center.

DOSAGE & ADMINISTRATION

Directions ▪ wet hands thoroughly with product and rub into skin until dry.▪ Children under 6 years of age should be supervised by an adult. when using this product.

INACTIVE INGREDIENT

Inactive ingredients Water, Aloe Barbadensis Leaf Juice, Carbomer,Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate (Vitamin E), Triethanolamine

SPL UNCLASSIFIED SECTION

KILLS GERMS*

ANTIBACTERIAL

with Moisturizers & Vitamin E

*Kills 99.9% of many common germs.

www.ostltrade.com

Imported by O.S.T.L.Inc

Made in P.R.C.

Packaging

INGREDIENTS AND APPEARANCE

CARE PLUS HAND SANITIZER 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69950-028
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
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
TROLAMINE (UNII: 9O3K93S3TK)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69950-028-02	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	06/17/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/17/2020

Labeler - Ostl, Inc. (020117798)