MDP PEPTIDE 9 BIO SUN PRO- homosalate, octocrylene, ethylhexyl salicylate, butyl methoxydibenzoylmethane stick

MDP PEPTIDE 9 BIO SUN PRO by

Drug Labeling and Warnings

MDP PEPTIDE 9 BIO SUN PRO by is a Otc medication manufactured, distributed, or labeled by SKINIDEA CO., LTD, Cosmax, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient(s)

Homosalate 9.50%

Octocrylene 5.00%

Ethylhexyl Salicylate 4.50%

Butyl Methoxydibenzoylmethane 2.70%

INACTIVE INGREDIENT

Inactive ingredients

Dimethicone, Methyl Methacrylate Crosspolymer, Synthetic Wax, Diethylhexyl Carbonate, Diisopropyl Sebacate, Diphenylsiloxy Phenyl Trimethicone, Isopropyl Palmitate, Polymethyl Methacrylate, Caprylyl Trimethicone, Diisostearyl Malate, Phenethyl Benzoate, Acrylates Copolymer, Bis-Behenyl/Isostearyl/Phytosteryl Dimer Dilinoleyl Dimer Dilinoleate, Butyloctyl Salicylate, Polyethylene, Dimethicone/Vinyl Dimethicone Crosspolymer, Microcrystalline Wax, Polymethylsilsesquioxane, Ethylene/Propylene Copolymer, Curcuma Longa (Turmeric) Root Extract, Silica Dimethyl Silylate, Dimethicone Crosspolymer, Fragrance(Parfum), Camellia Japonica Seed Oil, Melia Azadirachta Flower Extract, Melia Azadirachta Leaf Extract, Corallina Officinalis Extract, Melia Azadirachta Bark Extract, Moringa Oleifera Seed Oil, Ocimum Sanctum Leaf Extract, Water, Butylene Glycol, Hydrolyzed Hyaluronic Acid, Ectoin, Ubiquinone, Hydrogenated Polyisobutene, Glycerin, 1,2-Hexanediol, Collagen Amino Acids, Propanediol, Haematococcus Pluvialis Extract, Sorbitan Laurate, Collagen, Aloe Barbadensis Leaf Extract, Dioscorea Japonica Root Extract, Hydroxyethylcellulose, Laminaria Japonica Extract, Sodium Hyaluronate, Ulmus Davidiana Root Extract, Viola Mandshurica Flower Extract, Acetyl Dipeptide-1 Cetyl Ester, Heptasodium Hexacarboxymethyl Dipeptide-12, Hydroxypropyltrimonium Hyaluronate, Acetyl Hexapeptide-8, Anemarrhena Asphodeloides Root Extract, Ascorbic Acid Polypeptide, Dextran, Hexapeptide-9, Sodium Acetylated Hyaluronate, Tripeptide-1, Tocopherol, Hyaluronic Acid, Collagen Extract, Hydrolyzed Sodium Hyaluronate, Sodium Hyaluronate Crosspolymer, Potassium Hyaluronate, Acetyl Octapeptide-3, Acetyl Tetrapeptide-2, Acetyl Tetrapeptide-3, Acetyl Tetrapeptide-5, Acetyl Tetrapeptide-9, Carnosine, Copper Tripeptide-1, Nonapeptide-1, Palmitoyl Pentapeptide-4, Palmitoyl Tripeptide-1, Palmitoyl Tripeptide-5

PURPOSE

Purpose

Sunscreen

WARNINGS

Warnings

■ For external use only.

KEEP OUT OF REACH OF CHILDREN

INDICATIONS & USAGE

Use(s)

■ Helps prevent sunburn

■ If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

DOSAGE & ADMINISTRATION

Directions

For sunscreen use:

■ Apply liberally 15 minutes before sun exposure

■ Use a water-resistant sunscreen if swimming or sweating

■ Reapply at least every 2 hours

DESCRIPTION

Other Information

■ Protect the product in this container from excessive heat and direct sun

Questions?

■ Please send an email to the following address
skinidea@medipeel.com

72220-002-02: MDP PEPTIDE 9 BIO SUN STICK PRO (version 1)

72220-002-04: MDP PEPTIDE 9 BIO SUN STICK PRO (version 2)

INGREDIENTS AND APPEARANCE

MDP PEPTIDE 9 BIO SUN PRO 
homosalate, octocrylene, ethylhexyl salicylate, butyl methoxydibenzoylmethane stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72220-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	9.5 g  in 100 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	5 g  in 100 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	4.5 g  in 100 g
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	2.7 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
DIMETHICONE (UNII: 92RU3N3Y1O)
DIISOPROPYL SEBACATE (UNII: J8T3X564IH)
DIETHYLHEXYL CARBONATE (UNII: YCD50O0Z6L)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72220-002-02	1 in 1 CARTON	11/01/2024
1	NDC: 72220-002-01	20 g in 1 CONTAINER; Type 0: Not a Combination Product
2	NDC: 72220-002-04	1 in 1 CARTON	11/01/2024
2	NDC: 72220-002-03	20 g in 1 CONTAINER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	11/01/2024

Labeler - SKINIDEA CO., LTD (690416325)

Establishment
Name	Address	ID/FEI	Business Operations
Cosmax, Inc.		689049693	manufacture(72220-002)