NDC 73586-103 Daydream Cushion Gentle Light
Avobenzone, Homosalate, Octisalate, Titanium Dioxide Cream Topical

Product Information

Daydream Cushion Gentle Light is a human over the counter drug product labeled by Em Cosmetics Llc. The generic name of Daydream Cushion Gentle Light is avobenzone, homosalate, octisalate, titanium dioxide. The product's dosage form is cream and is administered via topical form.

Product Code73586-103
Proprietary Name What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Daydream Cushion Gentle Light
Non-Proprietary Name What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
Avobenzone, Homosalate, Octisalate, Titanium Dioxide
Product Type 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.
Human Otc Drug
Dosage FormCream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
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.
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
Em Cosmetics Llc
Labeler Code73586
FDA Application Number 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.
part352
Marketing Category 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.
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
10-06-2020
Listing Expiration Date 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.
12-31-2022
Exclude Flag 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".
N
NDC Code Structure

What are the uses for Daydream Cushion Gentle Light?


Product Packages

NDC 73586-103-11

Package Description: 12 g in 1 CONTAINER

Product Details

What are Daydream Cushion Gentle Light Active Ingredients?

An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

Daydream Cushion Gentle Light Active Ingredients UNII Codes

Daydream Cushion Gentle Light Inactive Ingredients UNII Codes

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.

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Daydream Cushion Gentle Light Labeling and Warnings

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Table of Contents



Active Ingredients



Avobenzone 1.5%

Homosalate 8.0%

Octisalate 3.0%

Titanium Dioxide 11.8%


Purpose



Sunscreen

Sunscreen


Uses



  • Helps prevent sunburn.
  • If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer, early skin aging by the sun.

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.


Otc - Keep Out Of Reach Of Children



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


Directions



  • Apply generously 15 minutes before sun exposure apply to all skin exposed to the sun. Use a water-resistant sunscreen if swimming or sweating.
    • Sun Protection Measures: Spending time in the sun increases your risk of skin cancer & early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF of 15 or higher and other sun protection measures including:
    •      limit time in the sun, especially from 10 a.m. - 2 p.m.
    •      wear long-sleeve shirts, pants, hats, and sunglasses

Other Information



  • PROTECT THE PRODUCT IN THIS CONTAINER FROM EXCESSIVE HEAT AND DIRECT SUN

Inactive Ingredients



WATER, CYCLOPENTASILOXANE, CAPRYLYL METHICONE, BUTYLENE GLYCOL, CETYL PEG/PPG-10/1 DIMETHICONE, CYCLOHEXASILOXANE, NIACINAMIDE, ISOAMYL LAURATE, DIPHENYLSILOXY PHENYL TRIMETHICONE, C12-15 ALKYL BENZOATE, VINYL DIMETHICONE/METHICONE SILSEQUIOXANE CROSSPOLYMER, SODIUM CHLORIDE, CARICA PAPAYA (PAPAYA) FRUIT EXTRACT, TREMELLA FUCIFORMIS (MUSHROOM) EXTRACT, ORYZA SATIVA (RICE) EXTRACT, LYCIUM BARBARUM FRUIT EXTRACT, CAMELIA SINENSIS LEAF EXTRACT, HYDROXYACETOPHENONE, TRIMETHYLSILOXYSILICATE, LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE, TRIHYDROXYSTEARIN, POLYPROPYLSILSESQUIOXANE, SORBITAN OLIVATE, SORBITAN SESQUIOLATE, SYNTHETIC BEESWAX, TRIETHOXYCAPRYLYLSILANE, DIPROPYLENE GLYCOL, 1,2-HEXANEDIOL, PROPYLENE CARBONATE, DIMETHICONE, DIMETHICONAL, DISTEARDIMONIUM HECTORITE, DISODIUM EDTA, CHLORPHENESIN, IRON OXIDES


Package Label.Principal Display Panel




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