DR. C. TUNA ACNE PORE PURIFYING TONER- salicylic acid liquid

Dr. C. Tuna Acne Pore Purifying Toner by

Drug Labeling and Warnings

Dr. C. Tuna Acne Pore Purifying Toner by is a Otc medication manufactured, distributed, or labeled by Farmasi US LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

ACTIVE INGREDIENT

Salicylic Acid 0.5%

PURPOSE

Acne Treatment

USE

For the treatment of acne.

WARNINGS

For external use only

When using this product

skin irritation and dryness is more likely to occur if you combine this product with other topical acne skincare products. If irritation occurs, only use one topical acne skincare product at a time. Avoid sun exposure and use a sunscreen. Avoid contact with the eyes, lips and mouth. If contact occurs, flush thoroughly with water. Skin irritation may occur, characterized by redness or tingling; if increased, discontinue use and seek medical advice.

Keep out of reach of children.

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

Do not use

if you have very sensitive skin or are sensitive to salicylic acid.

DIRECTIONS

After cleansing, apply to face with a soft cotton ball or pad. Avoid the eye area. Do not rinse. Follow with Acne Blemish Control Serum.

OTHER INFORMATION

Store at room temperature.

INACTIVE INGREDIENTS

Water/Aqua, Alcohol Denat, Propylene Glycol, Polysorbate 20, Glycerin, Butylene Glycol, Hamamelis Virginiana Water, Dehydroacetic Acid, Benzyl Alcohol, Glycolic Acid, Phenoxyethanol, Salix Alba Bark Water, Ethylhexylglycerin.

Questions or Comments?

info@farmasius.com Monday – Friday (9 a.m – 6 p.m. EST) (786) 238-7338 

Package Labeling:

125mL Package Labeling

INGREDIENTS AND APPEARANCE

DR. C. TUNA ACNE PORE PURIFYING TONER 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74690-009
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	5 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
GLYCERIN (UNII: PDC6A3C0OX)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)
DEHYDROACETIC ACID (UNII: 2KAG279R6R)
BENZYL ALCOHOL (UNII: LKG8494WBH)
GLYCOLIC ACID (UNII: 0WT12SX38S)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SALIX ALBA BARK VOLATILE OIL (UNII: PW3MX00JXN)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74690-009-01	1 in 1 BOX	01/20/2021
1		225 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 74690-009-02	1 in 1 BOX	07/25/2021
2		125 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M006	01/20/2021

Labeler - Farmasi US LLC (113303351)