NDC 59779-058 Camphor

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  2. Cvs
  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

Dosage Form: -

Product Type: 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.

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 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.

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.