Active Ingredients:
Benzalkanium Chloride .13%Allantoin .5%Benzyl Alcohol .5%
Shing-releev
FDA Label NDC 63287-420
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Merix Pharmaceutical Corp. for the product Shing-releev (NDC 63287-420). 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 active ingredients:, uses:, warnings:, keep out of reach of children:, directions:, dosage & administration, other ingredients, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Uses:
For the relive of symtoms associated with shingles including pain, Burning, Itching and tingling First aid to help guard against secondary skin infection due to shingles.
Warnings:
For external used only. Not for ingestion.
Do not used- in yeast infections- do not spray directly on the eyes
When using this product, may tingle on contact.
Stop used and ask doctor if - condition worsens- symptoms
last more then 7 days .
Keep Out Of Reach Of Children:
If swallowget medical help or contact a Poison Control Center right away.
Directions:
Use at first sign of irritation or itching.Adults and children 12 years or older. Clean without soap.apply liberally to clean dry area free of soap or cleanser residue.
Dosage & Administration
Apply to area as needed 3-4 times daily.Do not use cotton applicator.May be used with sterile bandage after area is dry.
Other Ingredients
.Methylparaben Potassium Sorbate (natural preservative ).
Propylparaben , Viracea (proprietary Echinacea purpurea extract),
water (purified)
Package Label.Principal Display Panel
Shing carton
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