NDC 42421-641 Innovative Skin Perfector Bb Broad Spectrum Spf15 Sunscreen (light/medium)

NDC Product Code 42421-641

NDC CODE: 42421-641

Proprietary Name: Innovative Skin Perfector Bb Broad Spectrum Spf15 Sunscreen (light/medium) 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: 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.

NDC Code Structure

  • 42421 - Emilia Personal Care Inc.
    • 42421-641 - Innovative Skin Perfector Bb Broad Spectrum Spf15 Sunscreen (light/medium)

NDC 42421-641-11

Package Description: 1 TUBE in 1 CARTON > 75 g in 1 TUBE

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Innovative Skin Perfector Bb Broad Spectrum Spf15 Sunscreen (light/medium) with NDC 42421-641 is a product labeled by Emilia Personal Care Inc.. The generic name of Innovative Skin Perfector Bb Broad Spectrum Spf15 Sunscreen (light/medium) is . The product's dosage form is and is administered via form.

Labeler Name: Emilia Personal Care Inc.

Dosage Form: -

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.

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)
  • TALC (UNII: 7SEV7J4R1U)
  • ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
  • MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
  • POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
  • CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
  • GLYCERYL MYRISTATE (UNII: 6992Y81827)
  • ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
  • DOCOSANOL (UNII: 9G1OE216XY)
  • MINERAL OIL (UNII: T5L8T28FGP)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
  • CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
  • NYLON-12 (UNII: 446U8J075B)
  • TROLAMINE (UNII: 9O3K93S3TK)
  • AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
  • FERROUS OXIDE (UNII: G7036X8B5H)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
  • ALLANTOIN (UNII: 344S277G0Z)
  • CAFFEINE (UNII: 3G6A5W338E)
  • ASCORBIC ACID (UNII: PQ6CK8PD0R)
  • EDETATE DISODIUM (UNII: 7FLD91C86K)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
  • HYALURONIC ACID (UNII: S270N0TRQY)

Product Labeler Information

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

Labeler Name: Emilia Personal Care Inc.
Labeler Code: 42421
Start Marketing Date: 01-10-2014 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: 12-31-2019 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: I 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.

Innovative Skin Perfector Bb Broad Spectrum Spf15 Sunscreen (light/medium) Product Label Images

Innovative Skin Perfector Bb Broad Spectrum Spf15 Sunscreen (light/medium) 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 Ingredient

Octinoxate 4.0%Titanium Dioxide 2.1%

Purpose

Sunscreen

Uses

  • •Helps prevent sunburn •If 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

  • •Apply liberally 15 minutes before sun exposure. •Reapply at least every 2 hours •Use water-resistant sunscreen if swimming or sweating •Children under 6 months: ask a doctor •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: 1.limit time in the sun, especially from 10 a.m. - 2 p.m. 2.wear long-sleeved shirts, pants, hats and sunglasses

Other Information

  • •protect the product in this container from excessive heat and direct sun

Inactive Ingredients

Water, talc, C12-15 alkyl benzoate, caprylic/capric triglyceride, potassium cetyl phosphate, cyclopentasiloxane, glyceryl myristate, isononyl isononanoate, behenyl alcohol, mineral oil, glycerin, propylene glycol, microcrystalline cellulose, cellulose gum, phenoxyethanol, ethylhexylglycerin, nylon-12, fragrance, triethanolamine, ammonium acroloyldimethyltaurate/VP copolymer, iron oxides, butylene glycol, allantoin, caffeine, ascorbic acid, disodium EDTA, tocopheryl acetate (vitamin E), BHT, hyaluronic acid.

* Please review the disclaimer below.