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Vicks vapofreeze pain relieving - Medication Information

Product NDC Code 84126-302
Drug Name

Vicks vapofreeze pain relieving

Type Brand
Active Ingredients
Camphor (synthetic) .036 g/g
Menthol .16 g/g
Route TOPICAL
Dosage Form CREAM
RxCUI drug identifier 2683201
Application Number M017
Labeler Name The Procter & Gamble Manufacturing Company
Packages
Package NDC Code Description
84126-302-03 1 tube in 1 carton (84126-302-03) / 85 g in 1 tube
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Overdosage of Vicks VapoFreeze PAIN RELIEVING

Information about signs, symptoms, and laboratory findings of acute ovedosage and the general principles of overdose treatment.
If swallowed, get medical help or contact a Poison Control Center right away.

Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredients Camphor 3.6% Menthol 16% Active ingredients Purpose Topical anesthetic Topical analgesic

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.
Directions adults and children over 12 years of age and older: apply to the affected area not more than 3 to 4 times daily wash hands thoroughly with soap and water after each use children under 12 years of age: ask a doctor Store at no greater than 25°C (77°F).

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients carbomer homopolymer, cetyl alcohol, cetyl palmitate, edetate disodium, fragrance, glycerin, isopropyl isostearate, PEG-100 stearate, sodium hydroxide, stearic acid, stearyl alcohol, water

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.
Use temporarily relieves minor pain aches and pains of muscles and joints associated with: arthritis simple backache strains sprains bruises provides penetrating pain relief

Purpose

Information about the drug product’s indications for use.
Active ingredients Purpose Topical anesthetic Topical analgesic

Spl product data elements

Usually a list of ingredients in a drug product.
Vicks VapoFreeze PAIN RELIEVING Camphor, Menthol WATER GLYCERIN STEARYL ALCOHOL CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) SODIUM HYDROXIDE CETYL ALCOHOL ISOPROPYL ISOSTEARATE CETYL PALMITATE EDETATE DISODIUM PEG-100 STEARATE MENTHOL MENTHOL CAMPHOR (SYNTHETIC) CAMPHOR (SYNTHETIC)

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.
PRINCIPAL DISPLAY PANEL - 3 OZ VICKS ® Vapo Freeze™ PAIN RELIEVING CREAM MENTHOL CAMPHOR PAIN RELIEF MUSCLES • JOINTS PENETRATING FORMULA WITH VICKS ® VAPORS NET WT 3 OZ (85 g) 302

Spl unclassified section

Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.
Drug Facts DIST. BY: PROCTER & GAMBLE, CINCINNATI, OH 45202

Do not use

Information about all contraindications for use. These contraindications are absolute and are intended for situations in which consumers should not use the product unless a prior diagnosis has been established by a doctor or for situations in which certain consumers should not use the product under any circumstances regardless of whether a doctor or health professional is consulted.
Do not use on wounds or on irritated or damaged skin with a heating pad

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.

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions? 1-855-446-4345

Stop use

Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.
Stop use and ask a doctor if condition worsens or symptoms persist for more than 7 days symptoms clear up and occur again within a few days redness is present or excessive skin irritation occurs you experience severe burning pain, swelling, or blistering where the product was applied

When using

Information about side effects that people may experience, and the substances (e.g. alcohol) or activities (e.g. operating machinery, driving a car) to avoid while using the drug product.
When using this product use only as directed. do not bandage tightly or use with medicated patch avoid contact with eyes and mucous membranes do not expose the area to local heat or direct sunlight a transient burning sensation may occur upon application but generally disappears in several days avoid applying into skin folds

Pregnancy or breast feeding

Pregnancy or Breast feeding
If pregnant or breast-feeding, ask a health professional 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.
Warnings For external use only

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