NDC 70157-005 Soft Focus City Suncreen Serum Broad Spectrum Spf 30 Supergoop

NDC Product Code 70157-005

NDC CODE: 70157-005

Proprietary Name: Soft Focus City Suncreen Serum Broad Spectrum Spf 30 Supergoop 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

  • 70157 - Baxter Laboratories Pty. Ltd.
    • 70157-005 - Soft Focus City Suncreen Serum Broad Spectrum Spf 30

NDC 70157-005-02

Package Description: 1 TUBE in 1 CARTON > 60 mL in 1 TUBE (70157-005-01)

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

NDC Product Information

Soft Focus City Suncreen Serum Broad Spectrum Spf 30 Supergoop with NDC 70157-005 is a product labeled by Baxter Laboratories Pty. Ltd.. The generic name of Soft Focus City Suncreen Serum Broad Spectrum Spf 30 Supergoop is . The product's dosage form is and is administered via form.

Labeler Name: Baxter Laboratories Pty. Ltd.

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)
  • CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
  • ISOSTEARYL NEOPENTANOATE (UNII: 411THY156Q)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • CYCLOMETHICONE 6 (UNII: XHK3U310BA)
  • POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
  • CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
  • CAPRYLYL GLYCOL (UNII: 00YIU5438U)
  • XANTHAN GUM (UNII: TTV12P4NEE)
  • PEG-40 STEARATE (UNII: ECU18C66Q7)
  • TRICONTANYL POVIDONE (UNII: N0SS3Q238D)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
  • PANTHENOL TRIACETATE, (+)- (UNII: 1206E8961B)
  • CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB)
  • ETHYL LINOLEATE (UNII: MJ2YTT4J8M)
  • CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
  • OLEYL ALCOHOL (UNII: 172F2WN8DV)
  • TOCOPHEROL (UNII: R0ZB2556P8)
  • EDETATE DISODIUM (UNII: 7FLD91C86K)
  • PANTHENOL (UNII: WV9CM0O67Z)
  • TROLAMINE (UNII: 9O3K93S3TK)
  • PENTYLENE GLYCOL (UNII: 50C1307PZG)
  • SODIUM LACTATE (UNII: TU7HW0W0QT)
  • LACTIC ACID (UNII: 33X04XA5AT)
  • SERINE (UNII: 452VLY9402)
  • UREA (UNII: 8W8T17847W)
  • SORBITOL (UNII: 506T60A25R)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • ALLANTOIN (UNII: 344S277G0Z)
  • FERRIC OXIDE RED (UNII: 1K09F3G675)
  • FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
  • FERROSOFERRIC OXIDE (UNII: XM0M87F357)

Product Labeler Information

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

Labeler Name: Baxter Laboratories Pty. Ltd.
Labeler Code: 70157
Start Marketing Date: 12-30-2014 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: 12-31-2018 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.

Soft Focus City Suncreen Serum Broad Spectrum Spf 30 Supergoop 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

Otc - Active Ingredient

Active Ingredients         PurposeAvobenzone 3%            SunscreenHomosalate 8%            SunscreenOctisalate 4%               SunscreenOctocrylene 2%            Sunscreen

Otc - Purpose

Uses Helps prevent sunburnIf used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer snd early skin aging caused by the sun

Otc - Keep Out Of Reach Of Children

Keep out of reach of children

Indications & Usage

Stop use and ask a doctor if rash occurs

Warnings

Warnings​For External Use onlyDo not use on damaged or broken skin​When using this product keep out of eyes. Rinse with water to remove.If swallowed, get medical help or contact a Poison Control Center right away.

Dosage & Administration

DirectionsApply two pumps to face and neckat least 15 minutes prior to sun exposure. Oil-free and fast absorbing, it's ideal for use alone or as a smoothing primer under the rest of your skincare regimen.  Use a water resistant sunscreen if swimming or sweatingReapply at least every 2 hoursChildren under 6 months: Ask a doctor

Inactive Ingredient

Inactive Ingredients Aqua, Cyclopentasilosiloxane, Isostearyl Neopentanoate, Glycerin, Cyclohexasiloxane, Ceteareth-20, Polypropylene, Cetearyl Alcohol, Caprylyl Glycol, Xanthan Gum, PEG-40 Stearate, Triacontanyl PVP, Silica, Ammonium Acryloyldimethyltaurate/VP Copolymer, Panthenyl Triacetate, Cetyl Dimethicone, Ethyl Linoleate, Caprylhydroxamic Acid, Oleyl Alcohol, Tocopherol, Disodium EDTA, Panthenol, Triethanolamine, Pentylene Glycol, Sodium Lactate, Lactic Acid, Serine, Urea, Sorbitol, Sodium Chloride, Allantoin, CI 77492, CI77491, CI77499

* Please review the disclaimer below.