TIME SECRET MINERAL PRESSED POWDER LIGHT OCHRE- octyl methoxycinnamate, titanium dioxide, zinc oxide powder

TIME SECRET Mineral Pressed Powder Light Ochre by

Drug Labeling and Warnings

TIME SECRET Mineral Pressed Powder Light Ochre by is a Otc medication manufactured, distributed, or labeled by MSH Inc., Nihon Kolmar Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Octyl Methoxycinnamate 5.63&

Titanium Dioxide 13.73%

Zinc Oxide 9.00%

Purpose

Sunscreen

Warnings

For external use only

Do not use

Do not use on broken or damaged skin

When using

When using this product keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor

Stop use and ask a doctor if rash or irritation occurs or lasts.

Keep out of reach of children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Apply liberally before sun exposure and as needed
• Children under 6 months of age: ask a doctor

Inactive Ingredients

mica, nylon-12, acrylates/ethylhexyl acrylate crosspolymer, synthetic fluorphlogopite, silica, dimetihicone, boron nitride, diphenylsiloxy phenyl trimethicone, magnesium myristate, dimethicone/vinyl dimethicone cross polymer, vinyl dimethicone/methicone s ilsesquioxane crosspo lymer, diethylamino hydroxybenzoyl hexyl benzoate, phenoxyethanol, stearic acid, trimethyl siloxysilicate, aluminum dimyristate, stearyl glycyrrhetinate, tocopherol, phytosteryl/octyldodecyl lauroyl glutamate, water, sodium hyaluronate, ceramide np, coral powder, limnanthes alba (meadow roam) seed oil, hydroxyapatite, glycerin, alcohol, sasa veitchii leaf extract, polysorbate 80, dextran, platinum powder, trifluoro acetyl tripeptide-2

Questions

Questions or Comments: Call Us 626-872-0164

PRINCIPAL DISPLAY PANEL

TimeSecret Mineral Pressed Powder Light Ochre.jpg

INGREDIENTS AND APPEARANCE

TIME SECRET MINERAL PRESSED POWDER LIGHT OCHRE 
octyl methoxycinnamate, titanium dioxide, zinc oxide powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72372-201
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	422.25 mg  in 7500 mg
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	1029.75 mg  in 7500 mg
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	675 mg  in 7500 mg

Inactive Ingredients
Ingredient Name	Strength
NYLON-12 (UNII: 446U8J075B)
MICA (UNII: V8A1AW0880)
DIMETHICONE (UNII: 92RU3N3Y1O)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72372-201-01	7500 mg in 1 CASE; Type 0: Not a Combination Product	06/19/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part352	06/19/2018

Labeler - MSH Inc. (691891271)

Registrant - MSH Inc. (691891271)

Establishment
Name	Address	ID/FEI	Business Operations
MSH Inc.		691891271	manufacture(72372-201)