PROACTIVPLUS SPF PROTECTION SPF 15

Manufacturer
THE PROACTIV COMPANY LLC | KIK Holdco Company Inc
Effective date
2017-12-03
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:23:30

Label at a glance#

ProductPROACTIVPLUS SPF PROTECTION SPF 15
Active ingredientOctinoxate, Octisalate, Octocrylene
Label structure11 sections

Indications and uses

helps prevent sunburn

Dosage and administration

apply liberally 15 minutes before sun exposure use a water resistant sunscreen if swimming or sweating reapply at least every 2 hours children under 6 months: Ask a doctor

Storage and handling

protect this product from excessive heat and direct sun

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Octinoxate 6%
Octisalate 4%
Octocrylene 2%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

  • helps prevent sunburn

Warnings

WARNINGS SECTION

For external use only

Skin Cancer/Skin Aging Alert

SPL UNCLASSIFIED SECTION

spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to prevent sunburn, not skin cancer or early skin aging.

Do not use

OTC - DO NOT USE SECTION

on damaged or broken skin.

When using this product

OTC - WHEN USING SECTION

keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor

OTC - STOP USE SECTION

if rash occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • apply liberally 15 minutes before sun exposure
  • use a water resistant sunscreen if swimming or sweating
  • reapply at least every 2 hours
  • children under 6 months: Ask a doctor

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, polyglyceryl-3 laurate, safflower oil/palm oil aminopropanediol esters, oligopeptide-51, morus alba leaf extract, camellia sinensis leaf extract, hamamelis virginiana (witch hazel) bark/leaf/twig extract, panthenol, allantoin, tocopherol, bisabolol, hydroxymethoxyphenyl decanone, cetearyl clcohol, dicetyl phosphate, ceteth-20 phosphate, glycerin, dimethicone/vinyl dimethicone crosspolymer, acrylates/C10-30 alkyl acrylate crosspolymer, isoceteth-10, silica, butylene glycol, aminomethyl propanol, cyclopentasiloxane, ethylhexylglycerin, tetrasodium EDTA, citric acid, sodium hydroxide, phenoxyethanol, fragrance

Other information

STORAGE AND HANDLING SECTION

  • protect this product from excessive heat and direct sun

Questions or comments?

OTC - QUESTIONS SECTION

Within US 1-800-950-4695

SPL UNCLASSIFIED SECTION

Distributed by The Proactiv Company LLC
100 N Sepulveda Blvd., El Segundo, CA 90245
proactiv.com ● Manufactured in Canada
Proactiv is a trademark of The Proactiv Company Sàrl

PRINCIPAL DISPLAY PANEL - 20 mL Tube Box

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

proactiv®        

LIQUID  SPF
SPF 15
SUNSCREEN
                 

0.75 FL. OZ. 20 mL

20_ml_carton_image
20_ml_carton_image

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 32 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11410-03411410-034-55

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 30 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
3ac88525-ccdc-4660-8484-e9dbf06d10079ad9ef52-34a5-4eee-be3e-cb58ea7deb362017-12-03WarningsExact identifier
spl id: 3ac88525-ccdc-4660-8484-e9dbf06d1007
spl set id: 9ad9ef52-34a5-4eee-be3e-cb58ea7deb36

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.