NDC 57913-2857 Oil-control Day Spf 15

  1. Labeler Index
  2. Erno Laszlo, Inc.
  3. NDC: 57913-2857 Oil-control Day Spf 15

NDC Product Code 57913-2857

NDC CODE: 57913-2857

Proprietary Name: Oil-control Day Spf 15 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

  • 57913 - Erno Laszlo, Inc.

NDC 57913-2857-8

Package Description: 1 BOTTLE in 1 CARTON > 90 mL in 1 BOTTLE

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

NDC Product Information

Oil-control Day Spf 15 with NDC 57913-2857 is a product labeled by Erno Laszlo, Inc.. The generic name of Oil-control Day Spf 15 is . The product's dosage form is and is administered via form.

Labeler Name: Erno Laszlo, Inc.

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)
  • BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
  • OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
  • ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
  • MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
  • GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • PEG-100 STEARATE (UNII: YD01N1999R)
  • SACCHARIDE ISOMERATE (UNII: W8K377W98I)
  • CETYL ALCOHOL (UNII: 936JST6JCN)
  • OCTYLDODECANOL (UNII: 461N1O614Y)
  • CETETH-20 (UNII: I835H2IHHX)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • SQUALANE (UNII: GW89575KF9)
  • ARACHIDYL PROPIONATE (UNII: QV5DAH3MSB)
  • ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
  • ETHYL LINOLENATE (UNII: T54Y8H042V)
  • VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • ETHYL OLEATE (UNII: Z2Z439864Y)
  • LINOLENIC ACID (UNII: 0RBV727H71)
  • SODIUM HYDROXIDE (UNII: 55X04QC32I)
  • LOCUST BEAN GUM (UNII: V4716MY704)
  • STEARETH-2 (UNII: V56DFE46J5)
  • POLYSORBATE 20 (UNII: 7T1F30V5YH)
  • EDETATE DISODIUM (UNII: 7FLD91C86K)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • O-CYMEN-5-OL (UNII: H41B6Q1I9L)

Product Labeler Information

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

Labeler Name: Erno Laszlo, Inc.
Labeler Code: 57913
Start Marketing Date: 04-10-2013 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 - INACTIVATED, the listing data was inactivated by the FDA. 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".

* Please review the disclaimer below.

Oil-control Day Spf 15 Product Label Images

Oil-control Day Spf 15 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

Other

Drug Facts

DISTRIBUTED IN U.S.A. BY ERNO LASZLO NEW YORK, NY 10001

Active Ingredients

Avobenzone 3.0%, Octinoxate 7.5%

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.

Otc - Do Not Use

Do not use on damaged or broken skin.

Otc - When Using

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

Otc - Stop Use

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 liberally 15 minutes before sun exposurereapply: after 40 minutes of swimming or sweatingimmediately after towel dryingat least every 2 hoursSun 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 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 sunglasseschildren under 6 months: Ask a doctor

Inactive Ingredients

Water, Butylene Glycol, Octyldodecyl Neopentanoate, C12-15 Alkyl Benzoate, Caprylic/Capric Triglyceride, Glyceryl Stearate, Glycerin, PEG-100 Stearate, Saccharide Isomerate, Cetyl Alcohol, Octyldodecanol, Ceteth-20, Dimethicone, Squalane, Arachidyl Propionate, Ascorbic Acid/Orange/Citrus Limon/Citrus Aurantifolia Polypeptides, Ascorbic Acid Polypeptide, Beta-Glucan, Ethylhexylglycerin, Ethyl Linolenate, Retinyl Palmitate, Tocopheryl Acetate, Ethyl Oleate, Lecithin, Linolenic Acid, Sodium Hydroxide, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Ceratonia Siliqua (Carob) Gum, Steareth-2, Polysorbate 20, Disodium EDTA, Phenoxyethanol, O-Cymen-5-Ol, Fragrance.

Other Information

  • Protect this product from excessive heat and direct sun

* Please review the disclaimer below.