EQUATE HAND SANITIZER WITH ALOE- ethyl alcohol gel
Wal-Mart Stores, 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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EQUATE HAND SANITIZER WITH ALOE

Active ingredient

ETHYL ALCOHOL 65%

Purpose

Antiseptic

Uses

Decreases 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 doctor if

irritation and redness develop
condition persists for more than 72 hours

Keep out of reach of children.

If swallowed, get medical hep or contact a Poison Control Center right away.

Directions

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

Other information

not store above 105°F
may discolor some fabrics
harmful to wood finishes and plastics

Inactive ingredient

water, glycerin, acrylates/c10-30 alkyl acrylate crosspolymer, triethanolamine, fragrance, aloe barbadensis leaf juice, maltodextrin, panthenol, blue 1, yellow 5

Questions?

1-888-287-1915

EQT_3oz_Aloe_GelHandSanitizer_V3

EQUATE HAND SANITIZER WITH ALOE
ethyl alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:49035-533
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	65 mL in 100 mL

Ingredient Name	Strength
Inactive Ingredients
water (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
TROLAMINE (UNII: 9O3K93S3TK)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
PANTHENOL (UNII: WV9CM0O67Z)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:49035-533-03	89 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/07/2020
2	NDC:49035-533-12	355 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/07/2020
3	NDC:49035-533-34	1000 mL in 1 BOTTLE; Type 0: Not a Combination Product	04/07/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	04/07/2020

Labeler - Wal-Mart Stores, Inc. (051957769)

Registrant - Wal-Mart Stores, Inc. (051957769)