OI LIN SUNMILK SUNSCREEN SPF 25

Dosage form: emulsion
Ingredients: TITANIUM DIOXIDE 85mg in 1g
Labeler: Sunrider Manufacturing L.P.
NDC Code: 62191-012

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.

OIL LIN® SUNMILK SUNSCREEN SPF 25

ACTIVE INGREDIENT: TITANIUM DIOXIDE 8.5%

INACTIVE INGREDIENT: WATER (DEIONIZED)

USES: HELPS PREVENT SUNBURN.

RECOMMENDATION: APPPLY EVENLY TO ANY AREA OF THE BODY BEFORE SUN EXPOSURE TO PROVIDE MODERATE PROTECTION AGAINST SUNBURN.  REAPPLY AS NEEDED OR AFTER PROLONGED PHYSICAL ACTIVITY OR SWIMMING.  HIGHER SPF GIVES MORE SUNBURN PROTECTION.  RETAINS SPF AFTER 40 MINUTES OF ACTIVITY IN THE WATER.  CHILDREN UNDER 6 MONTHS OF AGE:CONSULT A DOCTOR BEFORE USE.

WARNING:  FOR EXTERNAL USE ONLY, IF SWALLOWED SEEK MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY, IF CONTACT WITH EYES OCCURS, RINSE THOROUGHLY WITH WATER, DISCONTINUE USE AND CONSULT A DOCTOR IF PERSISTENT SIGNS OF IRRITATION OR RASH APPEAR

KEEP OUT OF REACH OF CHILDREN.

MM1
MM2
MM3


OI LIN SUNMILK SUNSCREEN SPF 25 
sunscreen, titanium dioxide emulsion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62191-012
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TITANIUM DIOXIDE (TITANIUM DIOXIDE) TITANIUM DIOXIDE85 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
2-HYDROXYETHYL ACRYLATE 
ALANINE 
ALOE VERA LEAF 
ALUMINUM HYDROXIDE 
ARGININE 
BETAINE 
BUTYLENE GLYCOL 
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 1.5) 
CYCLOMETHICONE 5 
DIMETHICONE 
EDETATE DISODIUM 
GLUTAMIC ACID 
GLYCINE 
HEXYL LAURATE 
HYALURONATE SODIUM 
isononyl isononanoate 
LYSINE 
OAT 
PHENOXYETHANOL 
POLYGLYCERYL-4 ISOSTEARATE 
POLYSORBATE 60 
PROLINE 
SERINE 
SODIUM CHLORIDE 
SODIUM HYDROXYMETHYLGLYCINATE  
SODIUM MYRISTOYL SARCOSINATE 
SODIUM PYRROLIDONE CARBOXYLATE 
SORBITOL 
SQUALANE 
THREONINE 
WATER 
Packaging
#Item CodePackage Description
1NDC:62191-012-0115 g in 1 TUBE
2NDC:62191-012-02125 g in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35204/23/2009
Labeler - Sunrider Manufacturing L.P. (786951475)
Registrant - Sunrider Manufacturing L.P. (786951475)

Revised: 02/2013
 
Sunrider Manufacturing L.P.

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 combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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