NDC 56062-709 Publix Spf 30

NDC Product Code 56062-709

NDC 56062-709-16

Package Description: 226 g in 1 BOTTLE, PLASTIC

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

NDC Product Information

Publix Spf 30 with NDC 56062-709 is a product labeled by Publix Super Markets Inc. The generic name of Publix Spf 30 is . The product's dosage form is and is administered via form.

Labeler Name: Publix Super Markets 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)
  • SORBITOL (UNII: 506T60A25R)
  • PEG-100 STEARATE (UNII: YD01N1999R)

Product Labeler Information

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

Labeler Name: Publix Super Markets Inc
Labeler Code: 56062
Start Marketing Date: 07-16-2013 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.

Publix Spf 30 Product Label Images

Publix Spf 30 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

Avobenzone 2.0%Homosalate 10.0%Octisalate    5.0%Octocrylene 5.0%




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


For external use only

When Using This Product

  • Keep out of eyes. Rinse with water to remove.

Stop Use And Ask A Doctor If

Rash occurs

Otc - Keep Out Of Reach Of Children

Keep out of the reach of children.If swallowed get medical help or contact a Poison Control Center right away.May stain some fabrics


  • Apply literally 15 minutes before sun exposure    reapply: after 80 minutes of swimming or sweating    immediately after towel drying    at least every 2 hoursSun protection measures.Spending time in the sun increase 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 am - 2 pm    Wear long sleeves shirts, pants, hats and sunglasses    children under 6 month of age: Ask a doctor

Other Information

Protect this product from excessive heat and direct sun

Inactive Ingredients

Water, Ethylhexyl Plamitate, Sorbitol, Polyglyceryl-3 Methylglucose Distearate, Acrylates/C12-22 Alkyl Methacrylate Copolymer, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine, Glyceryl Stearate, PEG_100 Stearate,Disodium EDTA, Oleth-3, Tocopherol,Aloe Barbadensis Leaf juice Powder,Benzyl Alcohol, Chlorphenesin, Fragrance.

* Please review the disclaimer below.