CARE PLUS HAND SANITIZER 8OZ by OSTL, INC.

CARE PLUS HAND SANITIZER 8OZ by

Drug Labeling and Warnings

CARE PLUS HAND SANITIZER 8OZ by is a Otc medication manufactured, distributed, or labeled by OSTL, INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

CARE PLUS HAND SANITIZER 8OZ- ethyl alcohol gel 
OSTL, INC.

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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Drug Facts
Active ingredient

Ethyl Alcohol 62.0 percent

Purpose

Antimicrobial

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.

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 ingredients:

Water (Aqua), Glycerin, Propylene Glycol, Carbomer, Aminomethyl Propanol, Fragrance, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate (Vitamin E)

CARE PLUS HAND SANITIZER 8OZ 
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69950-027
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)	Â
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)	Â
ALOE VERA LEAF (UNII: ZY81Z83H0X)	Â
CARBOMER 934 (UNII: Z135WT9208)	Â
AMINOMETHYL PROPANEDIOL (UNII: CZ7BU4QZJZ)	Â
GLYCERIN (UNII: PDC6A3C0OX)	Â
WATER (UNII: 059QF0KO0R)	Â

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69950-027-01	236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	06/01/2020

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

Labeler - OSTL, INC. (020117798)

Registrant - OSTL, INC. (020117798)

Revised: 6/2020

Document Id: a8cd107f-7978-b5c6-e053-2995a90ab860

34390-5

Set id: a8cd134c-0f6f-9313-e053-2a95a90a0131

Version: 1

Effective Time: 20200601

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