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I-MAX EXCELLENCE

Dosage form: lotion
Ingredients: AVOBENZONE 2.5g in 100mL, OCTINOXATE 7.5g in 100mL, OXYBENZONE 5g in 100mL
Labeler: MAXLIFE USA, INC.
NDC Code: 42952-101

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

I-MAX EXCELLENCE

ACTIVE INGREDIENTS:

AVOBENZONE 2.5%

OCTINOXATE 7.5%

OXYBENZONE 5%

PURPOSE:

SUNSCREEN

USES:

HELPS PREVENT SUNBURNS. HIGHER SPF GIVES MORE SUNBURN PROTECTION.

KEEP OUT OF REACH OF CHILDREN.


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

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 TypeHUMAN OTC DRUGItem Code (Source)NDC:42952-101
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AVOBENZONE (AVOBENZONE) AVOBENZONE2.5 g  in 100 mL
OCTINOXATE (OCTINOXATE) OCTINOXATE7.5 g  in 100 mL
OXYBENZONE (OXYBENZONE) OXYBENZONE5 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage Description
1NDC:42952-101-1259 mL in 1 BOTTLE
2NDC:42952-101-2259 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35203/15/2012
Labeler - MAXLIFE USA, INC. (785111431)
Registrant - MAXLIFE USA, INC. (785111431)

Revised: 05/2012
Document Id: 613d8dc2-aebb-4d6b-8e7b-dd0071db0af3
Set id: 0a654c5f-32c0-4599-91c3-1f17877aa8cb
Version: 6
Effective Time: 20120531
 
MAXLIFE USA, INC.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date, and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

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