MAXCLINIC HYALURONIC MESO CHANGE ROLLER- hyaluronic acid patch

MAXCLINIC HYALURONIC MESO CHANGE by

Drug Labeling and Warnings

MAXCLINIC HYALURONIC MESO CHANGE by is a Otc medication manufactured, distributed, or labeled by N&B LAB.Co.Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient: Hyaluronic acid 97.0%

INACTIVE INGREDIENT

Inactive Ingredients: Lactose

PURPOSE

Purpose: Skin Firming & Moisturizing

WARNINGS

Warnings: For external use only. Do not use on damaged or broken skin. When using this product keep out of eyes. Rinse with water to remove. Stop use and ask a doctor if rash occurs. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN

Directions

Directions: 1. First place the handle on the roller, then remove the protective cap. 2. Gently roll across the entire face for absorption. For optimal results, start rolling from areas with deep wrinkles (neck, smile lines, forehead). 3. Use for 3~5 minutes until the hyaluronic acid melts into the skin and then the roller becomes blunt. * First apply the ampoule on the face and neck, then use the roller. * Intended for a single use only. Please remove and discard the roller after use. * Once opened, use immediately

DOSAGE & ADMINISTRATION

Dosage & Administration: Use once a week.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MAXCLINIC HYALURONIC MESO CHANGE  ROLLER
hyaluronic acid patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69058-600
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYALURONIC ACID (UNII: S270N0TRQY) (HYALURONIC ACID - UNII:S270N0TRQY)	HYALURONIC ACID	67.9 mg  in 70 mg

Inactive Ingredients
Ingredient Name	Strength
Lactose (UNII: J2B2A4N98G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69058-600-02	4 in 1 CARTON	12/20/2016
1	NDC: 69058-600-01	70 mg in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		12/20/2016

Labeler - N&B LAB.Co.Ltd (690332858)

Registrant - N&B LAB.Co.Ltd (690332858)

Establishment
Name	Address	ID/FEI	Business Operations
N&B LAB.Co.Ltd		690332858	manufacture(69058-600)