NDC 50718-0033 Clear Acne Face Moisturizer

Acne Face Moisturizer

NDC Product Code 50718-0033

NDC 50718-0033-1

Package Description: 1 BOTTLE in 1 CARTON > 50 mL in 1 BOTTLE

NDC Product Information

Clear Acne Face Moisturizer with NDC 50718-0033 is a a human over the counter drug product labeled by Kamedis. The generic name of Clear Acne Face Moisturizer is acne face moisturizer. The product's dosage form is lotion and is administered via topical form.

Labeler Name: Kamedis

Dosage Form: Lotion - An emulsion, liquid1 dosage form. This dosage form is generally for external application to the skin.2

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.

Clear Acne Face Moisturizer 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.

  • SALICYLIC ACID 28.8 mg/mL

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.

  • ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)
  • ALCOHOL (UNII: 3K9958V90M)
  • ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)
  • ASCORBYL TETRAISOPALMITATE (UNII: 47143LT58A)
  • SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
  • BENZYL ALCOHOL (UNII: LKG8494WBH)
  • CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ)
  • CETYL ALCOHOL (UNII: 936JST6JCN)
  • PURSLANE (UNII: M6S840WXG5)
  • CHLORPHENESIN (UNII: I670DAL4SZ)
  • RHEUM PALMATUM ROOT (UNII: G025DAL7CE)
  • CHRYSANTHEMUM INDICUM FLOWER (UNII: I6OER6U04L)
  • DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • HEXYLENE GLYCOL (UNII: KEH0A3F75J)
  • PICEA ABIES WOOD (UNII: 72GZ8K8996)
  • PROPANEDIOL (UNII: 5965N8W85T)
  • SARCOSINE (UNII: Z711V88R5F)
  • WATER (UNII: 059QF0KO0R)
  • XANTHAN GUM (UNII: TTV12P4NEE)
  • CINNAMON BARK OIL (UNII: XE54U569EC)
  • SHEA BUTTER (UNII: K49155WL9Y)
  • SODIUM HYDROXIDE (UNII: 55X04QC32I)
  • PHYTATE SODIUM (UNII: 88496G1ERL)
  • SQUALANE (UNII: GW89575KF9)
  • STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
  • DOCOSANOL (UNII: 9G1OE216XY)
  • PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)
  • DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)
  • CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)
  • NORI (UNII: 477TV3P5UX)

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: Kamedis
Labeler Code: 50718
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: 01-01-2018 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: 12-31-2021 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 - NO 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Clear Acne Face Moisturizer Product Label Images

Clear Acne Face Moisturizer 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

Salicylic acid 2.0%

Purpose

Acne Treatment

Use

  • For the treatment of acne

Warnings

For external use only

When Using This Product

  • Avoid unnecessary sun exposure and usesunscreen.Avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water.Using other topical acne medication at the same time or immediately following the use of this product may increase dryness or irritation of the skin. If this occurs, only one medication at a time should be used, unless otherwise directed by a doctor.

Stop Use And Ask A Doctor

  • If irritation persists

Keep Out Of Reach Of Children

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

Directions

  • Cleanse the skin thoroughly before applying medication.Cover the entire affected area with a thin layer one to three times daily.Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor.If bothersome dryness or peeling occurs, reduce application to once a day or every other day.For children under 10 years of age, consult your physician.

Inactive Ingredients

Alcohol, Arachidyl Alcohol, Arachidyl Glucoside, Ascorbyl Tetraisopalmitate, Baikal Skullcap (Scutellaria Baicalensis) Root Extract, Behenyl Alcohol, Benzyl Alcohol, Capryloyl Glycine, Carbomer, Cetyl Alcohol, Chlorphenesin, Chinese Rhubarb (Rheum Palmatum) Root Extract, Chrysanthemum (Chrysanthemum Indicum) Flower Extract, Cinnamon (Cinnamomum Zeylanicum) Bark Extract, Common Purslane (Portulaca Oleracea) Extract, Dicaprylyl Carbonate, Fragrance, Glucose, Glycerin, Hexylene Glycol, Norway Spruce (Picea Abis) Extract, Phenethyl Alcohol, Plankton Extract, Propanediol, Sarcosine, SD Alcohol 40-C, Shea Butter (Butyrospermum Parkii), Sodium Hydroxide, Sodium Phytate, Squalane, Stearyl Alcohol, Water, Xanthan Gum.

* Please review the disclaimer below.