Rexall Vanishing Scent Pain Relieving
FDA Label NDC 55910-602

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Dolgencorp, Llc for the product Rexall Vanishing Scent Pain Relieving (NDC 55910-602). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding otc - active ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Active Ingredient

Active ingredient                                 PurposeMenthol 2.5%.................................................Topical Analgesic

Otc - Purpose

Uses temporarily relieves the minor aches and pains of muscles and joints associated with - simple backache - atrhritis - strains - bruises - sprains

Otc - Keep Out Of Reach Of Children

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

Indications & Usage

Uses temporarily relieves the minor aches and pains of muscles and joints associated with - simple backache - atrhritis - strains - bruises - sprains

Warnings

Warnings For external use onlyDo not use- on wounds or damaged skin- with a heating pad- on a child under 12 years of age with arthritis-like conditionsAsk a doctor before use if you have redness over the affected area.When using this product- avoid contact with the eyes or mucous membranes- do not bandage tightlyStop 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- excessive skin irritation occurs.Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Dosage & Administration

DirectionsAdults and children 12 years of age and older - apply to the affected area not more than 3 to 4times daily.Children under 12 years of age - consult a doctor

Inactive Ingredient

Inactive Ingredientspurified water, isopropyl alcohol, potassium hydroxide, non0xynol-9, carbomer, camphor, diazolidinyl urea

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