TATTOO GOO TATTOO MINERAL SUNSCREEN SPF 30- zinc oxide cream

Tattoo Goo Tattoo Mineral Sunscreen SPF 30 by

Drug Labeling and Warnings

Tattoo Goo Tattoo Mineral Sunscreen SPF 30 by is a Otc medication manufactured, distributed, or labeled by The Magni Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

Zinc Oxide** 12.5%

Purpose

Sunscreen

Uses

Helps prevent sunburn

Warnings

For external use only

Do not use

on damaged or broken skin. Allow new tattoos to heal for 3 weeks before use.

When using this product

keep out of eyes. Rinse with water to remove.

Stop use & ask doctor

if rash occurs.

Keep out of the reach of children.

If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

* apply liberally 15 minutes before sun exposure 

* use a water resistant sunscreen if swimming or sweating

* immediately after towel drying

* at least every 2 hours.

Inactive Ingredients

Water (Aqua), Coco-Caprylate/Caprate, Caprylic/Capric Triglyceride, Ethylhexyl Methoxycrylene, Glycerin, Calcium Sodium Borosilicate, Polyhydroxystearic Acid, Cetearyl Alcohol, Phenoxyethanol, Cetearyl Glucoside, C14-22 Alcohols, Hydrolyzed Soy Fiber, C12-20 Alkyl Glucoside, Xanthan Gum, Fructooligosaccharides, Beta Vulgaris (Beet) Root Extract, Ethylhexylglycerin, Sodium Phytate, Tocopheryl Acetate, Potassium Lactate, Lactic Acid, Tetrahexyldecyl Ascorbate.

Other information

Protect this product from excessive heat and direct sun

* may stain fabrics.

Package Labelling:

INGREDIENTS AND APPEARANCE

TATTOO GOO TATTOO MINERAL SUNSCREEN SPF 30 
zinc oxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 43689-0060
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	125 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)
GLYCERIN (UNII: PDC6A3C0OX)
CALCIUM SODIUM BOROSILICATE (UNII: 4MM76N4WMY)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
C14-22 ALCOHOLS (UNII: B1K89384RJ)
C12-20 ALKYL GLUCOSIDE (UNII: K67N5Z1RUA)
XANTHAN GUM (UNII: TTV12P4NEE)
BEET (UNII: N487KM8COK)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
PHYTATE SODIUM (UNII: 88496G1ERL)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
POTASSIUM LACTATE (UNII: 87V1KMK4QV)
LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)
TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 43689-0060-1	59 mL in 1 TUBE; Type 0: Not a Combination Product	08/20/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	08/20/2024

Labeler - The Magni Company (113501902)