NDC 59779-406 Cvs Cold Sore Treatment

NDC Product Code 59779-406

NDC CODE: 59779-406

Proprietary Name: Cvs Cold Sore Treatment 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.

NDC Code Structure

  • 59779 - Cvs Pharmacy

NDC 59779-406-01

Package Description: 1 TUBE in 1 PACKAGE > 2 g in 1 TUBE

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Cvs Cold Sore Treatment with NDC 59779-406 is a product labeled by Cvs Pharmacy. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 1094748.

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.

  • ALCOHOL (UNII: 3K9958V90M)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • ARGININE (UNII: 94ZLA3W45F)
  • BUTYLPARABEN (UNII: 3QPI1U3FV8)
  • CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
  • CETEARYL ISONONANOATE (UNII: P5O01U99NI)
  • DIPROPYLENE GLYCOL CAPRATE/CAPRYLATE DIESTER (UNII: R6G12EY23X)
  • ETHYLPARABEN (UNII: 14255EXE39)
  • CORYMBIA CITRIODORA LEAF OIL (UNII: M63U6N96EB)
  • HEXYLDECANOL (UNII: 151Z7P1317)
  • HEXYLDECYL LAURATE (UNII: 0V595C1P6M)
  • LEVOMENTHOL (UNII: BZ1R15MTK7)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • CERESIN (UNII: Q1LS2UJO3A)
  • TEA TREE OIL (UNII: VIF565UC2G)
  • POLOXAMER 407 (UNII: TUF2IVW3M2)
  • PROPYLPARABEN (UNII: Z8IX2SC1OH)
  • ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
  • THYMOL (UNII: 3J50XA376E)
  • ZINC CHLORIDE (UNII: 86Q357L16B)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Cvs Pharmacy
Labeler Code: 59779
Start Marketing Date: 05-17-2011 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: 12-31-2018 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: I - INACTIVATED, the listing data was inactivated by the FDA. 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.

Cvs Cold Sore Treatment Product Label Images

Cvs Cold Sore Treatment 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

Benzalkonium Chloride 0.13%

Purpose

Cold Sore/Fever Blister Treatment/First Aid Antiseptic

Uses

  • For treatment of cold sores/fever blisters on the face or lipsHelps relieve the symptoms of itching, burning and pain associated with cold sores/fever blisters in just one dayRelieves dryness and softens cold sores and fever blistersFirst aid to help protect against infection in minor cuts, scrapes, burns, and sores

Warnings

  • For external use only: Do not use in the
  • Eyes or apply over large areas of the body. In case of deep or puncture
  • Wounds, animal bites or serious burns, consult a physician.Allergy Alert: Do not use if you are allergic to any of the ingredients in this product.When using this product avoid contact with eyes. Use only as directed.Stop use and consult a doctor if the condition persists or gets worse. Do not use longer than 1 week unless directed by a doctor.Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

Directions

  • Clean the affected areaApply a small amount of this product to the affected area 1 to 3 times dailyRub in gentlyWash hands before and after applying creamDo not share this product with anyoneChildren under 12 years of age: ask a doctor

Other Information

Store at room temperature

Inactive Ingredients

Alcohol, Aloe Barbadensis Leaf Juice, Arginine, Butylparaben, Camphor, Cetearylisononanoate, Dipropylenglycole Dicaprylate-Dicaprate, Ethylparaben, Eucalyptus Globulus Leaf Oil, Hexyldecanole, Hexyl Decyl Laurate, Menthol,Methylparaben, Ozokerite, Phenoxyethanol, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Poloxamer 407, Propylparaben, Tocopheryl Nicotinate (Vitamin E), Thymol, Zinc Chloride

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

* Please review the disclaimer below.