DESPICABLE ME BERRY- benzalkonium chloride gel

Despicable Me Berry by

Drug Labeling and Warnings

Despicable Me Berry by is a Otc medication manufactured, distributed, or labeled by Townley Inc., Foshan Jinxiong Technology Co ., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient

Benzalkonium Chloride 0.1%

PURPOSE

Purpose

Antibacterial

INDICATIONS & USAGE

Use

To decrease bacteria on the skin that could cause disease

DOSAGE & ADMINISTRATION

Directions

• Rub a dime sized drop into hands.
• For children under 6 use under adult supervision.

WARNINGS

Warnings

• For external use only - hands.
• Keep out of eyes. Avoid contact with broken skin.
• Stop use and ask a doctor if irritation or redness develops.
• Do not inhale or ingest. If swallowed, get medical help or contact a poison control center right away.

KEEP OUT OF REACH OF CHILDREN

keep out of reach of children

INACTIVE INGREDIENT

Inactive ingredients

water, glycerin, coceth-7, PPG-1-PEG-9 lauryl glycol ether, carbomer, sodium hydroxide, PEG-40 hydrogenated castor oil, fragrance, may contain: red 40, red 33, blue 1, yellow 5.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DESPICABLE ME BERRY 
benzalkonium chloride gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58737-205
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
FD&C RED NO. 40 (UNII: WZB9127XOA)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
COCETH-7 (UNII: 58Y261JLH5)
PPG-1-PEG-9 LAURYL GLYCOL ETHER (UNII: 5R8J43K25L)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
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: 58737-205-01	59 g in 1 BOTTLE; Type 0: Not a Combination Product	04/28/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/28/2017

Labeler - Townley Inc. (016956158)

Establishment
Name	Address	ID/FEI	Business Operations
Foshan Jinxiong Technology Co ., Ltd.		544328419	manufacture(58737-205)