Active Ingredient(S)
Artemisia extract [fhfi] 3%
Shingles Pain Relief Cream
FDA Label NDC 81799-009
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ehy Holdings Llc for the product Shingles Pain Relief Cream (NDC 81799-009). 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 ingredient(s), purpose, use, warnings, do not use, otc - when using, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
for shingles skin care
Use
For the treatment of symptomsof shingles, hives, and rashes.
Warnings
FOR EXTERNAL USE ONLY
Do Not Use
it on pregnant womenand children under 12 years ofage unless directed by a doctor
Otc - When Using
avoid contact with eyeslf contact occurs, rinse the eyesthoroughly with water.
Otc - Stop Use
condition worsens or does notimprove after regular use asdirected
Otc - Keep Out Of Reach Of Children
If swallowed, getmedical help or contact aPoison Control Center(1-800-222-1222) right away.
Directions
Apply a small amount to theproblem areas with circularmotions for 3 minutes till theskin absorbs the cream.
Apply it 2-3 times a day for thebest result.
Other Information
Store at room temperature andout of direct sunlight
Inactive Ingredients
Water, Sophora Flavescens Root,Cnidium Monnieri Fruit, KochiaScoparia Pollen, Dictamnus Dasyca-rpus Root, Smilax Glabra Whole
Otc - Ask Doctor
if you are allergic to ingredientsin this product.
Otc - Questions
Visit www.roycederm.com
Package Label - Principal Display Panel
81799-009-01
81799-009-01 (81799 009 01)
* Please review the disclaimer below.
