PROACTIV SOLUTION DAILY PROTECTION PLUS SUNSCREEN SPF 30- avobenzone, homosalate, octinoxate, octisalate, and oxybenzone cream 
THE PROACTIV COMPANY LLC

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.

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Proactiv Solution Daily Protection Plus Sunscreen SPF 30

Drug Facts

Active Ingredient

Avobenzone 2.0%, Homosalate 5.0%, Octinoxate 7.5%, Octisalate 5.0%, Oxybenzone 5.0%

Purpose

Sunscreen

Use

To protect against sun exposure

Warnings

For external use only

When using this product

  • avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if skin irritation develops and lasts.

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

Directions

  • Apply liberally and evenly to all areas 15 minutes before sun exposure
  • Reapply as needed after swimming or towel drying.
  • For children under 6 months of age, consult a doctor.

Inactive Ingredients

water (aqua), neopentyl glycol diheptanoate, trimethylpentanediol/adipic acid/glycerin crosspolymer, caprylic/capric triglyceride, silica, sodium acrylate/sodium acryloyldimethyl taurate copolymer, cetearyl alcohol, glyceryl stearate, PEG-100 stearate, tocopheryl acetate, retinyl palmitate, isononyl isononanoate, polysorbate 60, salicylic acid, phenoxyethanol, methylparaben, ethylparaben, butylparaben, propylparaben, isobutylparaben

PRINCIPAL DISPLAY PANEL - 112 g Tube Carton

Rodan & Fields

proactiv®
SOLUTION

Daily Protection Plus
Sunscreen

non-comedogenic

SPF
30

provides UVA/UVB protection

for face and body

4 OZ. 112 g

PRINCIPAL DISPLAY PANEL - 112 g Tube Carton
PROACTIV SOLUTION DAILY PROTECTION PLUS SUNSCREEN  SPF 30
avobenzone, homosalate, octinoxate, octisalate, and oxybenzone cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11410-405
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE2 mg  in 0.1 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE5 mg  in 0.1 g
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE7.5 mg  in 0.1 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE5 mg  in 0.1 g
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE5 mg  in 0.1 g
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11410-405-41112 g in 1 TUBE; Type 0: Not a Combination Product01/01/200412/31/2019
2NDC:11410-405-421 in 1 BOX01/01/200412/31/2019
2NDC:11410-405-41112 g in 1 TUBE; Type 0: Not a Combination Product
3NDC:11410-405-1748 g in 1 TUBE; Type 0: Not a Combination Product01/01/200412/31/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart35201/01/200412/31/2019
Labeler - THE PROACTIV COMPANY LLC (080216357)
Registrant - THE PROACTIV COMPANY LLC (080216357)

Revised: 7/2010
Document Id: 92d5fae1-863f-4aa5-9001-82b017de24e8
Set id: aae30d5c-186a-4d63-b4d7-09e4edc10f05
Version: 2
Effective Time: 20100707
 
THE PROACTIV COMPANY LLC