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

Menu
Search

Leader

Cardinal Health
Fruit of the Earth

Leader Dark Tanning SPF 4 Continuous Spray Sunscreen 6 fl oz - Drug Facts Label


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Octinoxate 2.0%, Oxybenzone 0.5%

Sunscreen

• 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 prevent sunburn, not skin cancer or early skin aging.

For external use only

  • do not use near heat, flame or while smoking
  • avoid long term storage above 104°F (40°C)

on damaged or broken skin

keep out of eyes. Rinse with water to remove. Do not puncture or incinerate. Contents under pressure. Do not store at temperatures above 120° F.

if rash occurs.

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

Directions

Apply liberally 15 minutes before sun exposure

Hold can 4-6 inches away from body, spray evenly to ensure complete coverage

Do not spray into face. Spray into hand and apply to face.

Use in well ventilated, but not windy areas

Reapply:

After 80 minutes of swimming or sweating

Immediately after towel drying

At least every 2 hours

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 of 15 or higher and other sun protection measures including:

limit time in the sun, especially from 10 am - 2 pm

wear long sleeve shirts, pants, hats, and sunglasses

Children under 6 months: ask a doctor

Alcohol denat., C12-15 alkyl benzoate, aloe barbadensis leaf juice, retinyl palmitate (vitamin A), ascorbic acid (vitamin C), tocopheryl acetate (vitamin E), daucus carota sativa (carrot) root extract, acrylates/octylacrylamide copolymer, fragrance

Questions or Comments?

Call toll free 1-800-200-6313

Label

LeaderLabel8.jpg

Leader

Octinoxate, Oxybenzone AEROSOL, SPRAY

Product Information

Product Type Human otc drug label Item Code (Source) NDC:37205-722
Route of Administration Topical DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 16.6 mg
OXYBENZONE OXYBENZONE 4.15 mg

Inactive Ingredients

Ingredient Name Strength
ALCOHOL
CARROT JUICE
C12-15 ALKYL BENZOATE
ASCORBIC ACID
VITAMIN A PALMITATE
.ALPHA.-TOCOPHEROL ACETATE
ALOE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:37205-722-30 177 in 1 CAN

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2012-01-15


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.