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

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Dr. C. Tuna Acne Pore Purifying Toner

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:

Label

125mL Package Labeling

125mL Label pt1125mL Label pt2125mL Inner Label pt2125mL Inner Label pt1

DR. C. TUNA ACNE PORE PURIFYING TONER 
salicylic acid liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:74690-009
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:74690-009-011 in 1 BOX01/20/2021
1225 mL in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:74690-009-021 in 1 BOX07/25/2021
2125 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00601/20/2021
Labeler - Farmasi US LLC (113303351)

Revised: 11/2023
Document Id: 09733cf3-4b2b-1f7a-e063-6394a90a5c2d
Set id: b8dcfaab-8c55-f23d-e053-2a95a90a8a01
Version: 3
Effective Time: 20231105
 
Farmasi US LLC