NDC 76485-1111 Rimmel Lasting Breathable Foundation Spf 20

Octinoxate

NDC Product Code 76485-1111

NDC Code: 76485-1111

Proprietary Name: Rimmel Lasting Breathable Foundation Spf 20 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.

Non-Proprietary Name: Octinoxate 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.


Code Structure
  • 76485 - Rimmel Inc.
    • 76485-1111 - Rimmel Lasting Breathable Foundation Spf 20

NDC 76485-1111-0

Package Description: 30 mL in 1 BOTTLE

NDC 76485-1111-1

Package Description: 30 mL in 1 BOTTLE

NDC 76485-1111-2

Package Description: 30 mL in 1 BOTTLE

NDC 76485-1111-3

Package Description: 30 mL in 1 BOTTLE

NDC 76485-1111-4

Package Description: 30 mL in 1 BOTTLE

NDC 76485-1111-5

Package Description: 30 mL in 1 BOTTLE

NDC 76485-1111-6

Package Description: 30 mL in 1 BOTTLE

NDC 76485-1111-7

Package Description: 30 mL in 1 BOTTLE

NDC 76485-1111-8

Package Description: 30 mL in 1 BOTTLE

NDC 76485-1111-9

Package Description: 30 mL in 1 BOTTLE

NDC Product Information

Rimmel Lasting Breathable Foundation Spf 20 with NDC 76485-1111 is a a human over the counter drug product labeled by Rimmel Inc.. The generic name of Rimmel Lasting Breathable Foundation Spf 20 is octinoxate. The product's dosage form is liquid and is administered via topical form.

Labeler Name: Rimmel Inc.

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

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.


Rimmel Lasting Breathable Foundation Spf 20 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.

  • OCTINOXATE 4 g/100mL

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.

  • ISODODECANE (UNII: A8289P68Y2)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
  • TALC (UNII: 7SEV7J4R1U)
  • PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • CHLORPHENESIN (UNII: I670DAL4SZ)
  • ASCORBYL PALMITATE (UNII: QN83US2B0N)
  • SODIUM HYDROXIDE (UNII: 55X04QC32I)
  • SODIUM LACTATE (UNII: TU7HW0W0QT)
  • TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN)
  • SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
  • TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
  • WATER (UNII: 059QF0KO0R)
  • PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
  • PENTYLENE GLYCOL (UNII: 50C1307PZG)
  • PROPYLENE CARBONATE (UNII: 8D08K3S51E)
  • ALLANTOIN (UNII: 344S277G0Z)

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.

Labeler Name: Rimmel Inc.
Labeler Code: 76485
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 NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. 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: 03-15-2019 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’.

* Please review the disclaimer below.

Rimmel Lasting Breathable Foundation Spf 20 Product Label Images

Rimmel Lasting Breathable Foundation Spf 20 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

Octinoxate 4%

Purpose

Sunscreen

Uses

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

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • For sunscreen use:apply liberally 15 minutes before sun exposurereapply at least every 2 hoursuse a water resistant sunscreen if swimming or sweating Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: [bullet] limit time in the sun, especially from 10 a.m.-2 p.m. [bullet] wear long-sleeved shirts, pants, hats, and sunglasses.Children under 6 months of age: ask a doctor

Other Information

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

Inactive Ingredients

WATER, CYCLOPENTASILOXANE, TALC, ISODODECANE, GLYCERIN, VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER, PHENYL TRIMETHICONE, PEG-10 DIMETHICONE, TRIMETHYLSILOXYSILICATE, SODIUM CHLORIDE, AMMONIUM ACRYLATES COPOLYMER, PHENOXYETHANOL, DISTEARDIMONIUM HECTORITE, PENTYLENE GLYCOL, TRIETHOXYCAPRYLYLSILANE, CHLORPHENESIN, FRAGRANCE, ALCOHOL DENAT., ASCORBYL PALMITATE, CITRIC ACID, FRUCTOSE, PROPYLENE CARBONATE, SODIUM HYDROXIDE, TOCOPHERYL ACETATE, UREA, RETINYL PALMITATE, DISODIUM DECETH-6 SULFOSUCCINATE, DISODIUM EDTA, LAURETH-30, ALLANTOIN, MALTOSE, SODIUM LACTATE, SODIUM PCA, TREHALOSE, SODIUM DEHYDROACETATE, BHT, GLUCOSE, SODIUM HYALURONATE, TOCOPHEROL, [May Contain: TITANIUM DIOXIDE, IRON OXIDES]

* Please review the disclaimer below.

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