Label: HYALURONIC ACID MICRO- hyaluronate sodium patch
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Updated August 6, 2015
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- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- KEEP OUT OF REACH OF CHILDREN
INDICATIONS & USAGE
Indications & usage:1. Take a patch out of the pouch with dry hand after face washing. 2. Try not to touch the middle side (needle) and take off the protective film carefully. 3. Place and attach the middle side of the patch on a desired area vertically. 4. Press the middle part of the patch attached with fingers several times. 5. Go to bed with patch attached and take it off the next morning.
- DOSAGE & ADMINISTRATION
- PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
INGREDIENTS AND APPEARANCE
HYALURONIC ACID MICRO
hyaluronate sodium patch
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70018-010 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYALURONATE SODIUM (UNII: YSE9PPT4TH) (HYALURONIC ACID - UNII:S270N0TRQY) HYALURONATE SODIUM 1.14 g in 4 Inactive Ingredients Ingredient Name Strength Lactose (UNII: J2B2A4N98G) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70018-010-01 4 in 1 CARTON; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 07/01/2015 Labeler - JUNMOK INTERNATIONAL,INC (689045829) Registrant - JUNMOK INTERNATIONAL,INC (689045829) Establishment Name Address ID/FEI Business Operations JUNMOK INTERNATIONAL,INC 689045829 manufacture(70018-010)