NDC 10157-8009 Fruit Smoothies

Product Information

Product Code10157-8009
Proprietary Name 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.
Fruit Smoothies
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
Blistex Inc.
Labeler Code10157
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
09-01-2013
Listing Expiration Date 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.
12-31-2019
Exclude Flag 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".
I
NDC Code Structure

Usage Information


Product Characteristics

Color(s)ORANGE (C48331)
GREEN (C48329)
PINK (C48328)

Product Packages

NDC 10157-8009-1

Package Description: 1 KIT in 1 BLISTER PACK * 2.83 g in 1 CYLINDER * 2.83 g in 1 CYLINDER * 2.83 g in 1 CYLINDER

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

Product Details

Fruit Smoothies is product labeled by Blistex Inc.. The product's dosage form is and is administered via form.


What are Fruit Smoothies Active Ingredients?

The following is the list of active ingredients in this product. An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

  • DIMETHICONE (UNII: 92RU3N3Y1O)
  • DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
  • OCTINOXATE (UNII: 4Y5P7MUD51)
  • OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
  • OXYBENZONE (UNII: 95OOS7VE0Y)
  • OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)


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.

  • ALUMINUM OXIDE (UNII: LMI26O6933)
  • YELLOW WAX (UNII: 2ZA36H0S2V)
  • DIETHYLHEXYL ADIPATE (UNII: MBY1SL921L)
  • GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
  • ETHYLHEXYL PALMITATE (UNII: 2865993309)
  • ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
  • MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
  • MYRISTYL MYRISTATE (UNII: 4042ZC00DY)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • HYDROGENATED COCONUT OIL (UNII: JY81OXM1OM)
  • ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
  • ISOPROPYL STEARATE (UNII: 43253ZW1MZ)
  • TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
  • TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
  • PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
  • HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
  • D&C RED NO. 30 (UNII: 2S42T2808B)
  • D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
  • SACCHARIN (UNII: FST467XS7D)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • ALUMINUM OXIDE (UNII: LMI26O6933)
  • YELLOW WAX (UNII: 2ZA36H0S2V)
  • DIETHYLHEXYL ADIPATE (UNII: MBY1SL921L)
  • GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
  • ETHYLHEXYL PALMITATE (UNII: 2865993309)
  • ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
  • MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
  • MYRISTYL MYRISTATE (UNII: 4042ZC00DY)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • HYDROGENATED COCONUT OIL (UNII: JY81OXM1OM)
  • ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
  • ISOPROPYL STEARATE (UNII: 43253ZW1MZ)
  • TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
  • TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
  • PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
  • HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
  • D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
  • SACCHARIN (UNII: FST467XS7D)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
  • ALUMINUM OXIDE (UNII: LMI26O6933)
  • YELLOW WAX (UNII: 2ZA36H0S2V)
  • DIETHYLHEXYL ADIPATE (UNII: MBY1SL921L)
  • GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
  • ETHYLHEXYL PALMITATE (UNII: 2865993309)
  • ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
  • MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
  • MYRISTYL MYRISTATE (UNII: 4042ZC00DY)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • HYDROGENATED COCONUT OIL (UNII: JY81OXM1OM)
  • ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
  • ISOPROPYL STEARATE (UNII: 43253ZW1MZ)
  • TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)
  • TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
  • PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)
  • HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
  • D&C RED NO. 30 (UNII: 2S42T2808B)
  • SACCHARIN (UNII: FST467XS7D)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)


* Please review the disclaimer below.

Fruit Smoothies Labeling and Warnings

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Table of Contents



Other



Drug Facts

For external use only


Otc - Purpose



Active ingredientsPurpose
Dimethicone 1.0% (w/w) Lip protectant
Octinoxate 7.5% (w/w) Sunscreen
Oxybenzone 2.5% (w/w) Sunscreen

Uses



  • temporarily protects and helps relieve chapped or cracked lips
  • helps prevent sunburn

Skin Cancer/Skin Aging Alert



Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to help prevent sunburn, not skin cancer or early skin aging.


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


Package Warning



CHOKING HAZARD. Has removable cap. Not for children under 3 years.


Otc - Keep Out Of Reach Of Children



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
  • reapply at least every 2 hours
  • use a water resistant sunscreen if swimming or sweating
  • children under 6 months of age: Ask a doctor

Other Information



  • protect the product in this container from excessive heat and direct sun

Inactive Ingredients



alumina, beeswax, blue 1 lake

May contain one or more of these ingredients.

, diethylhexyl adipate, ethylhexyl palmitate, ethylhexyl stearate, flavors, glyceryl stearate, hydrogenated coconut oil, isopropyl myristate, isopropyl palmitate, isopropyl stearate, jojoba esters, microcrystalline wax, myristyl myristate, phenoxyethanol, phenyl trimethicone, polyethylene, polyhydroxystearic acid, red 30 lake, saccharin, silica, tetrahexyldecyl ascorbate, titanium dioxide, tocopheryl acetate, yellow 10


Principal Display Panel - 3 Stick Blister Pack



SPF 15

NDC 10157-8009-1

Blistex®
LIP PROTECTANT/SUNSCREEN

Fruit
Smoothies®

3 Creamy Blends With Delicious
Fruit Flavors And Vitamins C&E

3 STICKS NET WT. .10 oz (2.83g) EACH


* Please review the disclaimer below.