NDC 00904-7851 Major Camphor And Phenol

NDC Product Code 00904-7851

NDC CODE: 00904-7851

Proprietary Name: Major Camphor And Phenol 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

  • 00904 - Major Pharmaceuticals

NDC 00904-7851-6

Package Description: 1 BOTTLE, PLASTIC in 1 CARTON > 44 mL in 1 BOTTLE, PLASTIC (00904-7851-7)

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

NDC Product Information

Major Camphor And Phenol with NDC 00904-7851 is a product labeled by Major Pharmaceuticals. 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: 308940.

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.


Product Labeler Information

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

Labeler Name: Major Pharmaceuticals
Labeler Code: 00904
Start Marketing Date: 05-09-2008 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: 12-31-2017 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.

Major Camphor And Phenol 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

Camphorated phenol(camphor, 10.8% and phenol, 4.7%)


Pain reliever/antiseptic


  • First aid to help reduce the risk of infection associated with minor cuts, scrapes, minor burns, and insect bitesfor the temporary relief of pain and itching associated with minor burns, sunbrun, minor cuts, scrapes, fever blisters and cold sores


  • For external use only

Do Not Use

  • In the eyesor apply over large areas of the body

Ask A Doctor Before Use If You Have

  • Deep or puncture woundsanimal bitesserious burns

When Using This Product

  • Avoid contact with the eyesdo not bandage

Stop Use And Ask Doctor If

  • Condition worsenssymptoms persist for more than 7 days or clear up and occur again within a few days

Keep Out Of Reach Of Children

If swallowed, get medical help or contact a Poison Control Center right away. Do not induce vomiting before contacting medical help or a Poison Control Center


  • Clean the affected areaadults and children 2 years of age or older: apply a small amount of this product on the area 1 to 3 times dailychildren under 2 years of age: consult a doctor

Inactive Ingredients

Eucalyptus oil, light mineral oil

* Please review the disclaimer below.