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ILLUMINATING DAILY MOISTURIZER SPF 30

Dosage form: lotion
Ingredients: HOMOSALATE 12.0000mL in 100mL, OCTISALATE 5.0000mL in 100mL, AVOBENZONE 3.0000mL in 100mL, OXYBENZONE 3.0000mL in 100mL, OCTOCRYLENE 1.7000mL in 100mL
Labeler: CVS PHARMACY INC
NDC Code: 59779-326

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.

DRUG FACTS BOX

ACTIVE INGREDIENTS
  • AVOBENZONE 3% (SUNSCREEN)
  • HOMOSALATE 12% (SUNSCREEN)
  • OCTISALATE 5% (SUNSCREEN)
  • OCTOCRYLENE 1.7% (SUNSCREEN)
  • OXYBENZONE 3% (SUNSCREEN)

USES AND DIRECTIONS
  • USES: HELPS PREVENT SUNBURN. HIGHER SPF GIVES MORE SUNBURN PROTECTION.
  • DIRECTIONS: APPLY EVENLY BEFORE SUN EXPOSURE. AFTER CLEANSING, SMOOTH OVER FACE AND NECK DAILY.

WARNINGS
  • FOR EXTERNAL USE ONLY.

WHEN USING THIS PRODUCT

AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE WITH WATER.

STOP USE AND ASK A DOCTOR IF

RASH OR REDNESS DEVELOPS AND LASTS.

KEEP OUT OF REACH OF CHILDREN

IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY.

OTHER INFORMATION

STORE AT ROOM TEMPERATURE.

PACKAGE LABELS/ Carton
  • Front and Back Labels: cvs2.5.jpg
  • Carton: cvs1.jpg
  • Carton: cvs2.jpg
ILLUMINATING DAILY MOISTURIZER  SPF 30
homosalate lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59779-326
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HOMOSALATE (HOMOSALATE) HOMOSALATE12.0000 mL  in 100 mL
OCTISALATE (OCTISALATE) OCTISALATE5.0000 mL  in 100 mL
AVOBENZONE (AVOBENZONE) AVOBENZONE3.0000 mL  in 100 mL
OXYBENZONE (OXYBENZONE) OXYBENZONE3.0000 mL  in 100 mL
OCTOCRYLENE (OCTOCRYLENE) OCTOCRYLENE1.7000 mL  in 100 mL
Packaging
#Item CodePackage Description
1NDC:59779-326-031 BOTTLE, PUMP (BOTTLE) in 1 CARTON
1NDC:59779-326-0074 mL in 1 BOTTLE, PUMP
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35208/04/2010
Labeler - CVS PHARMACY INC (062312574)

Revised: 08/2010
Document Id: 81bfb623-57f7-4a15-877f-5b2184a2e871
Set id: 652b6f1c-c4d9-4c01-9b68-9c0403d01c3c
Version: 1
Effective Time: 20100804
 
CVS PHARMACY 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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