Label: PEARSYS- sodium hyaluronate patch
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Contains inactivated NDC Code(s)
NDC Code(s): 72945-0003-1 - Packager: J World
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated December 1, 2021
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
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INDICATIONS & USAGE
spread water soluble cosmetics all over your face before using
open one sterilized micro chip roller for use
press the left pushbutton of the dedicated roller handle to insert a micro chip roller
gently rolls massages along the fact surface from inside to outside
use only until you feel no stimulation from the micro chip
after using, apply cosmetics evenly across face
after using, press the roller handle depressor to discard the micro chip roller (the micro chip roller is disposable)
dedicated roller handle keeps it clean with a continous use product
(this product is recommended to use one every 2 to 3 days)
- WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
PEARSYS
sodium hyaluronate patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72945-0003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYALURONATE SODIUM (UNII: YSE9PPT4TH) (HYALURONIC ACID - UNII:S270N0TRQY) HYALURONATE SODIUM 6.14 g in 100 g Inactive Ingredients Ingredient Name Strength ACETYL HEXAPEPTIDE-8 (UNII: L4EL31FWIL) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72945-0003-1 68 g in 1 PATCH; Type 0: Not a Combination Product 07/21/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 07/21/2019 Labeler - J World (690082781) Registrant - J World (690082781) Establishment Name Address ID/FEI Business Operations J World 690082781 manufacture(72945-0003) , label(72945-0003)
