Publix description, usages, side effects, indications, overdosage, supplying and lots more!

Menu
Search

Publix

Publix Super Markets Inc

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredients

Avobenzone 3.0%

Homosalate 13.0%

Octisalate    5.0%

Octocrylene 7.0%

Oxybenzone 4.0%


Purpose

Sunscreen


Publix Uses

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

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 occurs


Keep out of the reach of children.

If swallowed get medical help or contact a Poison Control Center right away.

May stain some fabrics.


Directions

  • apply literally 15 minutes before sun exposure
  • reapply: after 80 minutes of swimming or sweating
  • immediately after towel drying
  • at least every 2 hours

Sun 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, Sorbitol, Stearic Acid, Triethanolamine, Aluminum Starch Octenylsuccinate, Benzyl Alcohol, Sorbitan Isostearate, VP/Eicosene Copolymer, Dimethicone, Polyglyceryl-3 Distearate, Carbomer, Tocopherol, Disodium EDTA, Methylparaben, Propylparaben, Fragrance.


Principal Display Panel

Publix

sunscreen lotion

50 SPF

MOISTURIZING

VERY WATER RESISTANT

Broad Spectrum Protection

8 FL OZ(237 mL)Publix



Publix

AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:56062-703
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
AVOBENZONE AVOBENZONE 3 g
HOMOSALATE Homosalate 13 g
OCTISALATE OCTISALATE 5 g
OCTOCRYLENE Octocrylene 7 g
OXYBENZONE OXYBENZONE 4 g

Inactive Ingredients

Ingredient Name Strength
water
sorbitol
STEARIC ACID
TROLAMINE
ALUMINUM STARCH OCTENYLSUCCINATE
BENZYL ALCOHOL
Sorbitan Isostearate
DIMETHICONE
METHYLPARABEN
Tocopherol
PROPYLPARABEN
EDETATE DISODIUM

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:56062-703-16 226 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2013-07-12


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.