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

Magix

Avon Products, Inc

  • Description
  • Clinical Pharmacology
  • Indications & Usage
  • Contraindications
  • Warnings
  • Precautions
  • Side Effects
  • Overdosage
  • Dosage & Administration
  • How Supplied
  • Patient Counseling Information
  • Supplemental Patient Material
  • Boxed Warning
  • Patient Package Insert



FULL PRESCRIBING INFORMATION

Active ingredient

Active ingredients


Purpose

Purpose

..................................Sunscreen
..................................Sunscreen

Uses

Uses • helps prevent sunburn

Warnings
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.

For external use only

Do not use on damaged or broken skin

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 reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• apply liberally 15 minutes before sun exposure

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

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


Inactive ingredients:

Dimethicone, Cyclopentasiloxane, Calcium Sodium Borosilicate, Cellulose, Cetearyl Dimethicone Crosspolymer, Alumina, Acrylates/Dimethicone Copolymer, Silica, Nylon-12, HDI/Trimethylol Hexyllactone Crosspolymer, C30-45 Alkyl Methicone, C30-45 Olefin, PEG/PPG-20/23 Dimethicone, Lauryl PEG-9 Polydimethylsiloxyethyl Dimethicone, Caprylyl Glycol, Dimethicone Crosspolymer, Polyethylene, Parfum/Fragrance, Boron Nitride.

Questions or Comments?
Call toll free 1-800-FOR-AVON or 1-800-265-AVON in Canada

Magix

OCTINOXATE, OCTISALATE LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:10096-0158
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
OCTINOXATE OCTINOXATE 75 mg
OCTISALATE OCTISALATE 40 mg

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:10096-0158-1 30 in 1 TUBE
2 NDC:10096-0158-2 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2012-01-06


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