DR. C. TUNA ACNE BLEMISH CONTROL SERUM- salicylic acid liquid

Dr. C. Tuna Acne Blemish Control Serum by

Drug Labeling and Warnings

Dr. C. Tuna Acne Blemish Control Serum 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 1%

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

Apply 2-3 drops once a day where needed on clean skin. Avoid the eye area. Follow with Acne Balancing Cream.

OTHER INFORMATION

Store at room temperature.

INACTIVE INGREDIENTS

Water/Aqua, Propylene Glycol, Glycerin, Sodium PCA, Glycolic Acid, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Xanthan Gum, Hamamelis Virginiana Water, Dehydroacetic Acid, Benzyl Alcohol, Sodium Benzoate, Potassium Sorbate, Triethanolamine, Salix Alba Bark Water, Tocopheryl Acetate.

Questions or Comments?

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

Package Labeling:

INGREDIENTS AND APPEARANCE

DR. C. TUNA ACNE BLEMISH CONTROL SERUM 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74690-011
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	10 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
GLYCOLIC ACID (UNII: 0WT12SX38S)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
XANTHAN GUM (UNII: TTV12P4NEE)
DEHYDROACETIC ACID (UNII: 2KAG279R6R)
BENZYL ALCOHOL (UNII: LKG8494WBH)
SODIUM BENZOATE (UNII: OJ245FE5EU)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
TROLAMINE (UNII: 9O3K93S3TK)
SALIX ALBA BARK VOLATILE OIL (UNII: PW3MX00JXN)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74690-011-01	1 in 1 BOX	01/20/2021
1		30 mL in 1 BOTTLE, GLASS; 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)