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Product NDC Code | 76176-112 | ||||||
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Drug Name | Pharmacys prescription vapor rub |
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Type | Brand | ||||||
Active Ingredients |
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Route | TOPICAL | ||||||
Dosage Form | GEL | ||||||
RxCUI drug identifier | 1042788 | ||||||
Application Number | part341 | ||||||
Labeler Name | NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD. | ||||||
Packages |
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Active ingredient
A list of the active, medicinal ingredients in the drug product.Active Ingredients Menthol 1 percent Camphor 4.7 percent Eucalyptus Oil 1 percent
Dosage and administration
Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.USE: To temporarily relieve nasal congestion, chest congestion and cough due to the common cold. Temporarily relieves minor aches and pains.
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Inactive Ingredients: Petrolatum, Mineral Oil, Nutmeg Oil, Turpentine Oil, Thymol, Cedar Leaf Oil.
Indications and usage
A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.Directions: Adults and children 2 years of age and older rub a thick layer on chest and throat for temporary relief from nasal congestion and coughing due to colds or rub on sore, aching muscles. If desired, loosely cover with a soft dry cloth but keep clothing loose. Repeat up to three times daily, especially at bedtime. Children under 2 years of age, consult your physician.
Purpose
Information about the drug product’s indications for use.Purpose Decongestant
Spl product data elements
Usually a list of ingredients in a drug product.PHARMACYS PRESCRIPTION VAPOR RUB menthol PETROLATUM MINERAL OIL NUTMEG OIL TURPENTINE OIL THYMOL CEDAR LEAF OIL MENTHOL MENTHOL EUCALYPTUS OIL EUCALYPTUS OIL CAMPHOR (NATURAL) CAMPHOR (NATURAL)
Package label principal display panel
The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.1
Ask doctor or pharmacist
Information about when a doctor or pharmacist should be consulted about drug/drug or drug/food interactions before using a drug product.Consult a physician before use. If you have asthma, emphysema, persistent or chronic cough, cough associated with smoking or excessive mucus. If muscle aches persist for more than 7 days or comes back or if cough lasts more than 7 days, come back or occurs with fever, rash or a persistent headache.
Keep out of reach of children
Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.Keep out of reach of children. If ingested, seek medical help or contact a Posion Control Center right away.
Other safety information
Information about safe use and handling of the product that may not have been specified in another field.Do not use near open flame, in a microwave oven or in a container in which water is being heated except when adding to cold water in a hot steam vaporizer.
Pregnancy or breast feeding
Pregnancy or Breast feedingIf pregnant or breast feeding, consult a physician before use.
Warnings
Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.WARNING: For external use only. Not for internal use. Avoid contact with eyes. Do not put in mouth, nostrils or on wounds or damaged skin.
Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API