Tattoo Goo

Manufacturer: The Magni Group Inc | United Laboratories Manufacturing LLC
Effective date: 2020-08-26
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:26:24

Label at a glance#

ProductTattoo Goo

Active ingredientCHLOROXYLENOL

Label structure10 sections

Dosage and administration

NDC: 43689-0056-1

Label contents#

Full prescribing information#

Active Ingredient: Chloroxylenol 0.5% Purpose: Antibacterial

OTC - ACTIVE INGREDIENT SECTION

Tattoo Goo DFP 59.15 mlNDC: 43689-0056-1

Purpose: Antibacterial

OTC - PURPOSE SECTION

NDC: 43689-0056-1 Tattoo Goo DFP 59.15ml

Use: Helps eliminate germs on skin

INDICATIONS & USAGE SECTION

NDC: 43689-0056-1

Warnings: For external use only

WARNINGS SECTION

NDC: 43689-0056-1

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

OTC - WHEN USING SECTION

NDC: 43689-0056-1

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

OTC - STOP USE SECTION

NDC: 43689-0056-1

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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.

DOSAGE & ADMINISTRATION SECTION

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.

INACTIVE INGREDIENT SECTION

NDC:43689-0056-1

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 43689-0056-1 Tattoo Goo PDP 59.15ml

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
43689-0056-1	2023-01-30	C162847	48780-1	f386c649-ad08-0266-e053-dadaa90a7c1a	ada9d426-0e4c-203e-e053-2a95a90a8dfc

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
43689-0056-1	Tattoo Goo	59.15 mL in 1 TUBE	LIQUID	59.15		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
43689-0056	TATTOO GOO (CHLOROXYLENOL) LIQUID [THE MAGNI GROUP INC]	1	Legacy NDC, 1 package rows	20200901_ada9d426-0e4c-203e-e053-2a95a90a8dfc.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

Tattoo Goo
Chloroxylenol
SODIUM LAURETH SULFATE
ANHYDROUS CITRIC ACID
WATER
POLYQUATERNIUM-10 (1000 MPA.S AT 2%)
COCO MONOETHANOLAMIDE
COCAMIDOPROPYL BETAINE
POTASSIUM SORBATE
DIAZOLIDINYL UREA
SODIUM BENZOATE
OLIVE OIL POLYGLYCERYL-6 ESTERS
PROPANEDIOL
POLYETHYLENE GLYCOL, UNSPECIFIED

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
43689-0056	43689-0056-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
SODIUM LAURETH SULFATE	BPV390UAP0	IACT
ANHYDROUS CITRIC ACID	XF417D3PSL	IACT
CHLOROXYLENOL	0F32U78V2Q	ACTIB
WATER	059QF0KO0R	IACT
POLYQUATERNIUM-10 (1000 MPA.S AT 2%)	GMR4PEN8PK	IACT
COCO MONOETHANOLAMIDE	C80684146D	IACT
COCAMIDOPROPYL BETAINE	5OCF3O11KX	IACT
POTASSIUM SORBATE	1VPU26JZZ4	IACT
DIAZOLIDINYL UREA	H5RIZ3MPW4	IACT
SODIUM BENZOATE	OJ245FE5EU	IACT
OLIVE OIL POLYGLYCERYL-6 ESTERS	4KDO9AFM9I	IACT
PROPANEDIOL	5965N8W85T	IACT
POLYETHYLENE GLYCOL, UNSPECIFIED	3WJQ0SDW1A	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
ada9d426-0e4d-203e-e053-2a95a90a8dfc			ada9d426-0e4c-203e-e053-2a95a90a8dfc	2020-08-26	Warnings	Exact identifier spl id: ada9d426-0e4d-203e-e053-2a95a90a8dfc spl set id: ada9d426-0e4c-203e-e053-2a95a90a8dfc

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.