SWEET LOVE HAND SANITIZER BODYCOLOGY- alcohol liquid

sweet love hand sanitizer by

Drug Labeling and Warnings

sweet love hand sanitizer by is a Otc medication manufactured, distributed, or labeled by Wal-Mart Stores Inc, Landy International. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient   Purpose

Alcohol 75%             Antiseptic

Uses For hand washing to decrease bacteria on the skin.

Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

Discontinue use if irritation and redness develop. If condition persists for more than 72 hours, consult a doctor.

Warnings

For external use only.

FLAMMABLE. Keep away from flame or high heat.

When using this product.

Avoid contact with eyes. If contact occurs, flush eyes with water.

Avoid contact with broken skin.

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.

Inactive ingredients: Water (Aqua, Eau), Fragrance (Parfum), Propylene Glycol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triehanolamine, Gelatin, Tocopheryl Acetate, Aloe Barbadensis Leaf Juice, Ultramarines (CI 77007).

May Contain: FD&C Red No. 4 (CI 14700), FD&C Yellow No. 5 (CI 19140), FD&C Blue No. 1 (CI 42090), D&C Red No. 33 (CI 17200).

PRINCIPAL DISPLAY PANEL

bodycology hand sanitizer

Sweet Love

1 Fl Oz / 30 mL

INGREDIENTS AND APPEARANCE

SWEET LOVE HAND SANITIZER  BODYCOLOGY
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49035-108
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
TROLAMINE (UNII: 9O3K93S3TK)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GELATIN (UNII: 2G86QN327L)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ULTRAMARINE BLUE (UNII: I39WR998BI)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49035-108-02	1 in 1 PACKAGE
1	NDC: 49035-108-01	30 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	05/22/2013

Labeler - Wal-Mart Stores Inc (051957769)

Registrant - Wal-Mart Stores Inc (051957769)

Establishment
Name	Address	ID/FEI	Business Operations
Landy International		545291775	manufacture(49035-108)