NDC 72372-401 Time Secret Mineral Liquid Cushion Light Ochre

Titanium Dioxide

NDC Product Code 72372-401

NDC 72372-401-01

Package Description: 11000 mg in 1 CASE

NDC Product Information

Time Secret Mineral Liquid Cushion Light Ochre with NDC 72372-401 is a a human over the counter drug product labeled by Msh Inc.. The generic name of Time Secret Mineral Liquid Cushion Light Ochre is titanium dioxide. The product's dosage form is powder and is administered via topical form.

Labeler Name: Msh Inc.

Dosage Form: Powder - An intimate mixture of dry, finely divided drugs and/or chemicals that may be intended for internal or external use.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Time Secret Mineral Liquid Cushion Light Ochre Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • TITANIUM DIOXIDE 1510 mg/11000mg

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • WATER (UNII: 059QF0KO0R)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Msh Inc.
Labeler Code: 72372
FDA Application Number: part352 What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 05-31-2019 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2020 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

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Time Secret Mineral Liquid Cushion Light Ochre Product Label Images

Time Secret Mineral Liquid Cushion Light Ochre Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients

Titanium Dioxide 13.73%




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.


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

Inactive Ingredients

Cyclopentasiloxane, water, diphenylsiloxy phenyl trimethicone, ethylhexyl methoxycinnamate, pentylene glycol, lauryl peg-10 tris(trimethylsiloxy)silylethyl dimethicone, triethylhexanoin, phenylbenzimidazole sulfonic acid, cetyl peg/ppg-10/1 dimethicone, disteardimonium hectorite, butyloctyl salicylate, diethylamino hydroxybenzoyl hexyl benzoate, bis-ethylhexyloxyphenol methoxyphenyl triazine, butyrospermum parkii(shea)oil, sodium chloride, butylene glycol, mica, trimethylsiloxysilicate, sodium hydroxide, phenoxyethanol, vinyl dimethicone/methicone silsesquioxane crosspolymer, hdi/trimethylol hexyllactone crosspolymer, tocopherol, dimethicone/vinyl dimethicone crosspolymer, silica silylate, ceramide np, coral powder, rosa canina fruit oil, glycerin, sodium hyaluronate, , dextran, trifluoroacetyl tripeptide-2, talc, iron oxides, dimethicone, aluminum hydroxide, hydrated silica, methicone, hydrogen dimethicone, silica, alumina


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