NDC 56062-708 Publix Spf 30

NDC Product Code 56062-708

NDC 56062-708-16

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 56062-708 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.

  • BENZYL ALCOHOL (UNII: LKG8494WBH)
  • SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)
  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • TOCOPHEROL (UNII: R0ZB2556P8)
  • PROPYLPARABEN (UNII: Z8IX2SC1OH)
  • EDETATE DISODIUM (UNII: 7FLD91C86K)
  • WATER (UNII: 059QF0KO0R)
  • SORBITOL (UNII: 506T60A25R)
  • TROLAMINE (UNII: 9O3K93S3TK)
  • STEARIC ACID (UNII: 4ELV7Z65AP)
  • BARIUM SULFATE (UNII: 25BB7EKE2E)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • JOJOBA OIL (UNII: 724GKU717M)

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: 11-15-2012 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 2.0%Oxybenzone 2.0%

Purpose

Sunscreen

Uses

  • Helps prevent sunburnhigher SPF gives more sunburn protectionretains SPF after 80 minutes of activity in water

Warnings

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 or irritation develops or lasts.

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.

Directions

  • Shake wellapply generously and evenly before sun exposure and as neededchildren under 6 months of age: ask a doctorreapply frequently and after towel drying, swimming or perspiring

Other Information

  • May stain some materials

Inactive Ingredients

Water, Sorbitan Isostearate, Sorbitol, Polyglyceryl-3 Distearate, Triethanolamine, Stearic Acid, VP/Eicosene Copolymer, Benzyl Alcohol, Dimethicone, Barium Sulfate, Carbomer, Simmondsia Chinensis (Jojoba) Seed Oil, Tocopherol, Disodium EDTA, Octadecene/MA Copolymer, Aloe Barbadensis Leaf Extract, Methylparaben, Propylparaben, Fragrance.

* Please review the disclaimer below.