IM DERMA RELIEF SUNSTICK- octocrylene, ethylhexyl methoxycinnamate, ethylhexyl salicylate stick

IM DERMA RELIEF SUNSTICK by

Drug Labeling and Warnings

IM DERMA RELIEF SUNSTICK by is a Otc medication manufactured, distributed, or labeled by Normalest Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

IM DERMA RELIEF SUNSTICK 
octocrylene, ethylhexyl methoxycinnamate, ethylhexyl salicylate stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72284-0010
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	1.05 g  in 15 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	1.2 g  in 15 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	0.675 g  in 15 g

Inactive Ingredients
Ingredient Name	Strength
HYALURONIC ACID (UNII: S270N0TRQY)
CENTELLA ASIATICA (UNII: 7M867G6T1U)
DIMETHICONE (UNII: 92RU3N3Y1O)
PARAFFIN (UNII: I9O0E3H2ZE)
TRIETHYLHEXANOIN (UNII: 7K3W1BIU6K)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE (UNII: ANQ870JD20)
PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE (UNII: 75D21FL1PI)
VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER (UNII: 9NH1UDD2RR)
MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
CANDELILLA WAX (UNII: WL0328HX19)
METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q)
BEMOTRIZINOL (UNII: PWZ1720CBH)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
POLYGLYCERYL-10 OLEATE (UNII: 55C81W76DH)
GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
ADENOSINE (UNII: K72T3FS567)
MADECASSOSIDE (UNII: CQ2F5O6YIY)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)

Product Characteristics
Color		Score
Shape	ROUND	Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72284-0010-1	1 in 1 BOX	12/05/2019
1		15 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 not final	part352	12/05/2019

Labeler - Normalest Co., Ltd. (694812877)

Registrant - Normalest Co., Ltd. (694812877)

Establishment
Name	Address	ID/FEI	Business Operations
Normalest Co., Ltd.		694812877	manufacture(72284-0010)