ADVANCED HAND SANITIZER- alcohol gel

Advanced Hand Sanitizer by

Drug Labeling and Warnings

Advanced Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by CDMA, Vi-Jon, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethyl alcohol 70%

Purpose

Antiseptic

Uses

• to decrease bacteria on the skin that could cause disease
• recommended for repeated use

Warnings

For external use only: hands

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 or redness develops
• 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

• wet hands thoroghly with product and allow to dry without wiping
• for children under 6, use only under adult supervision
• not recommended for infants

Other information

• do not sore above 105⁰ F
• may discolor some fabrics
• harmful to wood finishes and plastics

Inactive ingredients

water, glyceryl caprylate/caprate, glycerin, isopropyl myristate, tocopheryl acetate, acrylates/C10-30 alkyl acrylate crosspolymer, fragrance, benzophenone-4

SPL UNCLASSIFIED SECTION

*This product is not manufactured or distributed by GOJO Industries, Inc, distributer of Purell Advanced Hand Sanitizer.

**Effective at eliminating more than 99.99% of many common harmful germs and bacteria in as little as 15 seconds*

Distributed by CDMA, Inc.

43157 W Nine Mile

Novi, MI 48357

www.qualitychoice.com

Questions: 800-935-2362

principal display panel

QC

Quality Choice

*Compare to Purell Advanced Hand Sanitizer

Advanced Hand Sanitizer

Original

Kills More Than 99.99% of Germs**

Leaves hands feeling soft

With Moisturizers & Vitamin E

2 FL OZ (59 mL)

INGREDIENTS AND APPEARANCE

ADVANCED HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63868-882
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)
GLYCERYL CAPRYLATE/CAPRATE (UNII: G7515SW10N)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)
SULISOBENZONE (UNII: 1W6L629B4K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63868-882-16	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/05/2021
2	NDC: 63868-882-34	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/05/2021
3	NDC: 63868-882-45	946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/05/2021
4	NDC: 63868-882-43	473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/05/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	10/05/2021

Labeler - CDMA (011920774)

Registrant - Consumer Product Partners, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091520	manufacture(63868-882)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091514	manufacture(63868-882)