NDC 59779-058 Camphor

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  3. NDC: 59779-058 Camphor

NDC Product Code 59779-058

NDC CODE: 59779-058

Proprietary Name: Camphor 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: 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.

NDC Code Structure

NDC 59779-058-01

Package Description: 1 BOTTLE, PLASTIC in 1 CARTON > 237 mL in 1 BOTTLE, PLASTIC

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

NDC Product Information

Camphor with NDC 59779-058 is a product labeled by Cvs. The generic name of Camphor is . The product's dosage form is and is administered via form.

Labeler Name: Cvs

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)
  • CEDRUS ATLANTICA BARK (UNII: ITP1Q41UPF)
  • EUCALYPTUS OIL (UNII: 2R04ONI662)
  • LAURETH-7 (UNII: Z95S6G8201)
  • MENTHOL (UNII: L7T10EIP3A)
  • NUTMEG OIL (UNII: Z1CLM48948)
  • POLOXAMER 124 (UNII: 1S66E28KXA)
  • CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
  • ENGLISH LAVENDER OIL (UNII: ZBP1YXW0H8)

Product Labeler Information

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

Labeler Name: Cvs
Labeler Code: 59779
Start Marketing Date: 05-19-2009 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".

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Camphor Product Label Images

Camphor 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

Otc - Active Ingredient

Active ingredient                            PurposeCamphor 6.2%.............................Cough Suppressant

Otc - Purpose

Active ingredient                     PurposeCamphor 6.2%..................Cough Suppressant______________________________________Uses temporarily relieves cough due to minor throatand bronchial irritation associated with a cold.

Otc - Keep Out Of Reach Of Children

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

Indications & Usage

Uses - temporarily relieves cough due to minor throatand bronchial irritation associated with a cold.

Warnings

Warnings If pregnant or breastfeeding consult a healthcare professional before use___________________________________________________Flammable Keep away from fire or flame_____________________________________________- for steam inhalation only - do not take by mouth____________________________________________________Ask a doctor before use if you have a persistent orchronic cough such as occurs with smoking, asthma, oremphysema, or if cough is accompanied by excessivephlegm (mucus)_____________________________________________________When using this product do not- heat  - microwave  - use near an open flame- add to hot water or any container where heatingwater except when adding to cold water only in a hot steam vaporizer. May cause splattering andresult in burns______________________________________________________Stop use and ask a doctor if-cough persists for more than one (1) week, tends torecur, or is accompanied by fever, rash or persistent headache. A persistent cough may be a sign of a serious condition______________________________________________________Keep out of reach of children. If swallowed, getmedical help or contact a Poison Control Centerimmediately______________________________________________________

Dosage & Administration

Directions- See Important warnings under "When using this product"- Adults and children 2 years and older:    use 1 tablespoon of solution directly for each quart    of water or 1-1/2 teaspoonful of solution for each    pint of water    - add solution directly to COLD water only in a hot     steam vaporizer    - follow manufacturer's directions for using vaporizer    - Breath in medicated vapors    - use up to 3 times daily or as directed by a doctor- For use with children under 2 years of age:    ask a doctor________________________________Other information - Close container tightly andstore at room temperature away from heat

Inactive Ingredient

Inactive Ingredients Dimethicone, Eucalyptus Globulus (Encalyptus Oil) Leaf Oil, Laureth-7, Menthol,Mys=ristica Fragrans (nutmeg) Kernal Oil, Poloxarner 124,SD Alcohol 40-B, Thuja Occidentalis (Cedar Leaf) Oil,Lavandula Angustifolia (Lavender) Oil

* Please review the disclaimer below.