I-MAX EXCELLENCE description, usages, side effects, indications, overdosage, supplying and lots more!

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I-MAX EXCELLENCE

MAXLIFE USA, INC.
MAXLIFE USA, 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

I-MAX EXCELLENCE




FULL PRESCRIBING INFORMATION

Active ingredient

ACTIVE INGREDIENTS:

AVOBENZONE 2.5%

OCTINOXATE 7.5%

OXYBENZONE 5%

Purpose

PURPOSE:

SUNSCREEN

Uses

USES:

HELPS PREVENT SUNBURNS. HIGHER SPF GIVES MORE SUNBURN PROTECTION.






WHEN USING THIS PRODUCT

KEEP OUT OF EYES. RINSE WITH WATER TO REMOVE.

STOP USE AND ASK A DOCTOR IF

A RASH OR IRRITATION DEVELOPS AND LASTS. IF SWALLOWED, GET

MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

DIRECTIONS

APPLY TO CLEAN SKIN 15 MINUTES BEFORE SUN EXPOSURE. REAPPLY

AFTER SWIMMING, EXCERCISING OR PERSPIRATION IN THE SUNLIGHT.

CHILDREN UNDER 6 MONTHS OF AGE: ASK A DOCTOR.

INACTIVE INGREDIENTS:

ALKYL BENZOATE, ACRYLATES/C10-30 ALKYL ACRYLATES CROSSPOLYMER, C12-15 GLYCERYL STEARATE, CETEARYL PHOSPHATE, ETHYLHEXYLGLYCERIN, MAGNESIUM ALUMINUM SILICATE, PHENOXYETHANOL, PROPYLENE GLYCOL, SODIUM HYDROXIDE, STEARETH-20, STEARYL ALCOHOL, TETRAHEXYLDECYL ASCORBATE, TOCOPHERYL ACETATE, WATER (AQUA).

QUESTIONS? 1-323-733-7033

I-MAX

EXCELLENCE

SPF 30

SUNSCREEN

SPF 30 FOR SKIN PROTECTION

2 FL OZ / 59 ML


I-MAX EXCELLENCE

AVOBENZONE OCTINOXATE OXYBENZONE LOTION

Product Information

Product Type Human otc drug label Item Code (Source) NDC:42952-101
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
AVOBENZONE AVOBENZONE 2.5 g
OCTINOXATE OCTINOXATE 7.5 g
OXYBENZONE OXYBENZONE 5 g

Inactive Ingredients

Ingredient Name Strength
ALKYL (C12-15) BENZOATE
CARBOMER INTERPOLYMER TYPE A (55000 MPA.S)
GLYCERYL MONOSTEARATE
CETYL PHOSPHATE
ETHYLHEXYLGLYCERIN
magnesium aluminum silicate
PHENOXYETHANOL
propylene glycol
SODIUM HYDROXIDE
Steareth-20
stearyl alcohol
TETRAHEXYLDECYL ASCORBATE
ALPHA-TOCOPHEROL ACETATE
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:42952-101-12 59 in 1 BOTTLE
2 NDC:42952-101-22 59 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part352 2012-03-15


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Be sure to consult your doctor before taking any medication!
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