YOU ARE MY SUNSHINE ANTIBACTERIAL HAND SANITIZER WATERMELON SCENTED- alcohol gel

You Are My Sunshine Antibacterial Hand Sanitizer Watermelon Scented by

Drug Labeling and Warnings

You Are My Sunshine Antibacterial Hand Sanitizer Watermelon Scented by is a Otc medication manufactured, distributed, or labeled by Ganzhou Olivee Cosmetic Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

Ethyl Alcohol 65% 

Purpose

 Antiseptic

Use

Decrease bacteria on hands.

Warnings

For external use only.

Flammable.Keep product away from fire or flame.

When using this product

avoid contact with eyes; in case of contact, flush eyes with water.

Stop use and ask a doctor if

irritation or redness develops and persists.

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.

Inactive ingredients

Water (Aqua), ACRYLATES/C10-30 ALKYL ACRYLATE CROSSCOPOLYMER, AMINOMETHYL PROPANOL, Fragrance (Parfum), May contain: D&C Red No. 33 (Cl 17200), FD&C Red No. 4 (Cl 14700), FD&C Yellow No. 5 (Cl 19140), FD&C Blue No. 1 (Cl 42090).

SPL UNCLASSIFIED SECTION

No Animal Testing

Packaging

INGREDIENTS AND APPEARANCE

YOU ARE MY SUNSHINE ANTIBACTERIAL HAND SANITIZER WATERMELON SCENTED 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 56136-424
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)

Other Ingredients
Ingredient Kind	Ingredient Name	Quantity
May contain	D&C RED NO. 33 (UNII: 9DBA0SBB0L)
May contain	FD&C RED NO. 4 (UNII: X3W0AM1JLX)
May contain	FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
May contain	FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 56136-424-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/18/2020
2	NDC: 56136-424-02	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/18/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	10/18/2020

Labeler - Ganzhou Olivee Cosmetic Co., Ltd. (543008195)

Establishment
Name	Address	ID/FEI	Business Operations
Ganzhou Olivee Cosmetic Co., Ltd.		543008195	manufacture(56136-424)