Dr. C. Tuna Acne Blemish Control Serum

Manufacturer
Farmasi US LLC
Effective date
2023-11-05
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:59:06

Label at a glance#

ProductDr. C. Tuna Acne Blemish Control Serum
Active ingredientSALICYLIC ACID
Label structure8 sections

Dosage and administration

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

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 1%

PURPOSE

OTC - PURPOSE SECTION

Acne Treatment

USE

INDICATIONS & USAGE SECTION

For the treatment of acne.

WARNINGS

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Do not use

OTC - DO NOT USE SECTION

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

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

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

OTHER INFORMATION

SPL UNCLASSIFIED SECTION

Store at room temperature.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

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?

OTC - QUESTIONS SECTION

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

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Updated inner labelUpdated inner labelupdated label pt1updated label pt1updated label pt2updated label pt2

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1047362salicylic acid 1 % Topical SolutionPSN4
1047362salicylic acid 10 MG/ML Topical SolutionSCD4
1047362salicylic acid 1 % Topical SolutionSY4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74690-011-01Dr. C. Tuna Acne Blemish Control Serum30 mL in 1 BOTTLE, GLASSLIQUID304
74690-011-01Dr. C. Tuna Acne Blemish Control Serum1 in 1 BOXLIQUID14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74690-011DR. C. TUNA ACNE BLEMISH CONTROL SERUM (SALICYLIC ACID) LIQUID [FARMASI US LLC]4Current NDC, Legacy NDC, 2 package rows20231106_b8dd63d7-4ff2-60bc-e053-2a95a90ad16c.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74690-01174690-011-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Dr. C. Tuna Acne Blemish Control SerumSALICYLIC ACIDFarmasi US LLCb8dd63d7-4ff2-60bc-e053-2a95a90ad16c2023-11-05WarningsExact identifier
ndc (package): 74690-011-01
ndc (product): 74690-011
ndc11 (package): 74690001101
spl id: 09735173-2608-39fd-e063-6394a90aa6cf
spl set id: b8dd63d7-4ff2-60bc-e053-2a95a90ad16c

Reported adverse events (FAERS/openFDA)#

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