TATTOO GOO- chloroxylenol liquid

Tattoo Goo by

Drug Labeling and Warnings

Tattoo Goo by is a Otc medication manufactured, distributed, or labeled by The Magni Group Inc, United Laboratories Manufacturing LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient: Chloroxylenol 0.5% Purpose: Antibacterial

NDC: 43689-0056-1

Purpose: Antibacterial

NDC: 43689-0056-1

Use: Helps eliminate germs on skin

NDC: 43689-0056-1

Warnings: For external use only

NDC: 43689-0056-1

When using this product: -avoid contact with eyes -In case of eye contact, flush with water

NDC: 43689-0056-1

Stop use and ask a doctor if irritation or redness develops.

NDC: 43689-0056-1

Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

NDC: 43689-0056-1

Directions -Three to four times daily for tattoos, one to two times daily for piercings. -Squeeze into palm of hand. -Work up lather in hands. -Gently rub lather over tattoo or piercing. -Cold water rinse, pat, then air dry.

NDC: 43689-0056-1

Inactive Ingredients: Water (Aqua), Sodium PEG-7 Olive Oil Carboxylate, Propanediol, Olive Oil PEG-7 Esters, Sodium Laureth Sulfate, Polyquaternium 10, Cocoamide MEA, Cocamidopropyl Betaine, Diazolidinyl Urea, Sodium Benzoate, Potassium Sorbate, Citric Acid.

NDC: 43689-0056-1

Principal Display Panel

NDC: 43689-0056-1

INGREDIENTS AND APPEARANCE

TATTOO GOO 
chloroxylenol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 43689-0056
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	0.5 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
WATER (UNII: 059QF0KO0R)
POLYQUATERNIUM-10 (1000 MPA.S AT 2%) (UNII: GMR4PEN8PK)
COCO MONOETHANOLAMIDE (UNII: C80684146D)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
SODIUM BENZOATE (UNII: OJ245FE5EU)
OLIVE OIL POLYGLYCERYL-6 ESTERS (UNII: 4KDO9AFM9I)
PROPANEDIOL (UNII: 5965N8W85T)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 43689-0056-1	59.15 mL in 1 TUBE; Type 0: Not a Combination Product	08/25/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	08/25/2020

Labeler - The Magni Group Inc (113501902)

Establishment
Name	Address	ID/FEI	Business Operations
United Laboratories Manufacturing LLC		807878116	manufacture(43689-0056)