NDC 37012-626 Shopko Absolute Daily Moisturizing Broad Spectrum Spf15 Sunscreen

NDC Product Code 37012-626

NDC CODE: 37012-626

Proprietary Name: Shopko Absolute Daily Moisturizing Broad Spectrum Spf15 Sunscreen 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.

NDC Code Structure

  • 37012 - Shopko Stores Operating Co., Llc
    • 37012-626 - Shopko Absolute Daily Moisturizing Broad Spectrum Spf15 Sunscreen

NDC 37012-626-11

Package Description: 1 BOTTLE in 1 CARTON > 118 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

Shopko Absolute Daily Moisturizing Broad Spectrum Spf15 Sunscreen with NDC 37012-626 is a product labeled by Shopko Stores Operating Co., Llc. The product's dosage form is and is administered via form.

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)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
  • HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
  • ISOHEXADECANE (UNII: 918X1OUF1E)
  • POLYSORBATE 60 (UNII: CAL22UVI4M)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • CETYL ALCOHOL (UNII: 936JST6JCN)
  • CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
  • CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
  • PANTHENOL (UNII: WV9CM0O67Z)
  • NIACINAMIDE (UNII: 25X51I8RD4)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • ETHYLPARABEN (UNII: 14255EXE39)
  • PROPYLPARABEN (UNII: Z8IX2SC1OH)
  • STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
  • CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
  • DIMETHICONOL (100000 CST) (UNII: OSA9UP217S)
  • DOCOSANOL (UNII: 9G1OE216XY)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • DMDM HYDANTOIN (UNII: BYR0546TOW)
  • BENZYL ALCOHOL (UNII: LKG8494WBH)
  • PEG-4 DILAURATE (UNII: KCR71CW036)
  • STEARIC ACID (UNII: 4ELV7Z65AP)
  • PEG-100 STEARATE (UNII: YD01N1999R)
  • EDETATE DISODIUM (UNII: 7FLD91C86K)

Product Labeler Information

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

Labeler Name: Shopko Stores Operating Co., Llc
Labeler Code: 37012
Start Marketing Date: 06-01-2013 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.

Shopko Absolute Daily Moisturizing Broad Spectrum Spf15 Sunscreen Product Label Images

Shopko Absolute Daily Moisturizing Broad Spectrum Spf15 Sunscreen 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

Avobenzone 3.0%Homosalate 3.0%Oclisalate 5.0%Octocrylene 2.6%

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

  • Apply liberally 15 minutes before sun exposure.Children under 6 months of age: ask a doctorSun 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:limit time in the sun, especially from 10 a.m. - 2 p.m.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, glycerin, polyethylene, hydroxyethyl acrylate/sodium acryloyldimethyl taurate copolymer, isohexadecane, polysorbate 60, dimethicone, cetyl alcohol, cetearyl alcohol, cetearyl glucoside, panthenol (pro-vitamin B5), niacinamide, phenoxythanol, methylparaben, ethylparaben, propylparaben, stearyl alcohol, cyclopentasiloxane, dimethiconol, behenyl alcohol, tocopheryl acetate (vitamin E), DMDM hydantoin, benzyl alcohol, PEG-4 dilaurate, stearic acid, PEG-100 stearate, fragrance, disodium EDTA

* Please review the disclaimer below.