CPR HAND SANITIZER- ethyl alcohol liquid

CPR HAND SANITIZER by

Drug Labeling and Warnings

CPR HAND SANITIZER by is a Otc medication manufactured, distributed, or labeled by Cbd Research Labs, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient:

Ethyl Alcohol 70%

Purpose:

Antiseptic/ Antimicrobial

Uses:

To help reduce bacteria on the skin that could cause disease. Recommended for repeated use.

Warnings:

For external use only.

Flammable. Keep away from fire or flame

When using this product:

Keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest.

Stop use and ask a doctor if:

irritation and redness develops; if condition persists for more than 72 hours.

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

Directions:

Put enough product in your palms to cover hands and rub together briskly until dry. For children under 6, use only under adult supervision. Not recommended for infants.

Other Information:

Store below 110°F (43°C). May discolor some fabrics or surfaces. Harmful to wood finishes and plastics. 

Inactive Ingredients:

Water (Aqua), Aloe Barbadensis Leaf Juice, Glyceryl Caprylate/Caprate, Glycerin, Isopropyl Myristate, Tocopheryl Acetate, Acrylates, C10-30 Alkyl Acrylate Crosspolymer, Fragrance (Parfum), Benzephenone-4, Blue 1, Yellow 5.

SPL UNCLASSIFIED SECTION

Clean

Protect

Renew

Maximum Strength

Kills 99.99% of most common germs

Made in the U.S.A.

WWW.CBDRL.COM

Manufactured Exclusively for CPR

by CBD Research Labs, Inc.

Las Vegas, NV 89118

PARABEN FREE

NOT TESTED ON ANIMALS

Packaging

INGREDIENTS AND APPEARANCE

CPR HAND SANITIZER 
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73940-510
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)
GLYCERYL MONOCAPRYLATE (UNII: TM2TZD4G4A)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
SULISOBENZONE (UNII: 1W6L629B4K)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73940-510-02	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/10/2020
2	NDC: 73940-510-08	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/10/2020
3	NDC: 73940-510-16	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/10/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/10/2020

Labeler - Cbd Research Labs, Inc (117458248)