Quality Choice Advanced Hand Sanitizer with Aloe 439.001/439AC rev 1

Hand Sanitizer by

Drug Labeling and Warnings

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]

HAND SANITIZER- alcohol gel 
CDMA

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Quality Choice Advanced Hand Sanitizer with Aloe
439.001/439AC rev 1

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 heat and 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

• skin irritation 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 thoroughly with product and allow to dry witout wiping
• for children under 6, use only under adult supervision
• not recommended for infants

Other information

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

Inactive ingredients

water ,aloe barbadensis leaf juice,glyceryl caprylate/caprate ,glycerin ,isopropyl myristate ,tocopheryl acetate ,acrylates/C10-30 alkyl acrylate crosspolymer, fragrance ,benzophenone-4, blue 1, yellow 5

Questions?

1-888-593-0593

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

Distributed by CDMA, Inc.

43157 W Nine Mile

Novi, MI 48376

www.qualitychoice.com

Questions 800-935-2362

principal display panel

QC QUALITY CHOICE

Compare to Germ-X Advanced Hand Sanitizer with Aloe

Advanced

Hand Sanitizer

With Aloe

Kills More Than 99.99% of Germs*

Leaves hands feeling soft

With Moisturizer & Vitamin E

8 FL OZ (236 mL)

HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63868-439
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.7 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERYL CAPRYLATE/CAPRATE (UNII: G7515SW10N)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
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: 63868-439-34	236 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	10/05/2021	03/21/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	10/05/2021	03/21/2024

Labeler - CDMA (011920774)

Registrant - Consumer Product Partners, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091520	manufacture(63868-439)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091514	manufacture(63868-439)

Revised: 7/2024

Document Id: 1cd5d6c5-b19e-1178-e063-6394a90a0db6

34390-5

Set id: ac0e1491-aa50-4dbb-ae84-f50bda3fb37c

Version: 7

Effective Time: 20240709

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