NDC 74690-010 Dr. C. Tuna Acne Clear Complexion Cleanser
Salicylic Acid
NDC Product Code 74690-010
Proprietary Name: Dr. C. Tuna Acne Clear Complexion Cleanser What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name: Salicylic Acid What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
Drug Use Information
Drug Use InformationThe drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.
- Drug uses not available
NDC Code Structure
- 74690 - Farmasi Us Llc
- 74690-010 - Dr. C. Tuna Acne Clear Complexion Cleanser
NDC 74690-010-01
Package Description: 1 TUBE in 1 BOX > 100 mL in 1 TUBE
NDC Product Information
Dr. C. Tuna Acne Clear Complexion Cleanser with NDC 74690-010 is a a human over the counter drug product labeled by Farmasi Us Llc. The generic name of Dr. C. Tuna Acne Clear Complexion Cleanser is salicylic acid. The product's dosage form is gel and is administered via topical form.
Dosage Form: Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
Dr. C. Tuna Acne Clear Complexion Cleanser Active Ingredient(s)
What is the Active Ingredient(s) List?This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Inactive Ingredient(s)
About the Inactive Ingredient(s)The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.
- WATER (UNII: 059QF0KO0R)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
- SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
- PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
- DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
- GLYCOLIC ACID (UNII: 0WT12SX38S)
- GLYCERIN (UNII: PDC6A3C0OX)
- DEHYDROACETIC ACID (UNII: 2KAG279R6R)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- COCO GLUCOSIDE (UNII: ICS790225B)
- SALIX ALBA BARK VOLATILE OIL (UNII: PW3MX00JXN)
- TEA TREE OIL (UNII: VIF565UC2G)
- EDETATE SODIUM (UNII: MP1J8420LU)
- MENTHOL (UNII: L7T10EIP3A)
Administration Route(s)
What are the Administration Route(s)?The translation of the route code submitted by the firm, indicating route of administration.
- Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Product Labeler Information
What is the Labeler Name?Name of Company corresponding to the labeler code segment of the Product NDC.
Labeler Name: Farmasi Us Llc
Labeler Code: 74690
FDA Application Number: part333D What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
Marketing Category: OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
Start Marketing Date: 01-20-2021 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date: 12-31-2022 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.
Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.
* Please review the disclaimer below.
Dr. C. Tuna Acne Clear Complexion Cleanser Product Label Images
Dr. C. Tuna Acne Clear Complexion Cleanser Product Labeling Information
The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.
Product Labeling Index
- Active Ingredient
- Purpose
- Use
- Warnings
- When Using This Product
- Keep Out Of Reach Of Children.
- Do Not Use
- Directions
- Other Information
- Inactive Ingredients
Active Ingredient
Salicylic Acid 2%
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 to damp skin. Gently massage over face for 20-30 seconds. Avoid the eye area. Rinse thoroughly with warm water and pat dry. Follow with
Acne Pore Purifying Toner.
Other Information
Store at room temperature.
Inactive Ingredients
Water/Aqua, Cocomidopropyl Betaine, Ammonium Lauryl Sulfat, Sodium Laureth Sulfate, Propylene Glycol, Decyl Glucoside, PEG-150 Distearate,
Disodium Cocoamphodiacetate, Glycolic Acid, Glycerin, Hamamelis Virginiana Water, Dehydroacetic Acid, Benzyl Alcohol, Sodium Benzoate,
Potassium Sorbate, Styrene/Acrylates Copolymer, Coco-Glucoside, Salix Alba Bark Water, Tea Tree Oil/Melaleuca Alternifolia Leaf Oil, Tetrasodium EDTA, Menthol.
* Please review the disclaimer below.