Super CC Color Correction Care Primer Stick

Manufacturer
Grand Metro Cosmetics Company
Effective date
2016-01-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:29:26

Label at a glance#

ProductSuper CC Color Correction Care Primer Stick SPF 30
Active ingredientOXYBENZONE, ZINC OXIDE, OCTOCRYLENE, OCTINOXATE, TITANIUM DIOXIDE
Label structure11 sections

Dosage and administration

▪ Apply liberally 15 minutes before sun exposure ▪ Use a water resistant sunscreen if swimming or sweating ▪ Reapply: ▪ Immediately after towel drying • At least every 2 hours • Sun Protection Measures . Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF of 15 or higher and other sun protection measures includ...

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Octinoxate 5.6%, Titanium Dioxide 5.2%

Octocrylene 4.2% Zinc Oxide 4.0%

Oxybenzone 5.1%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Use

INDICATIONS & USAGE SECTION

▪ Helps prevent Sunburn. ▪ If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Warnings

WARNINGS SECTION

For external use only

Do not use on damaged or broken skin

When using this product

OTC - WHEN USING SECTION

▪ Keep out of eyes ▪ Rinse with water to remove

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.  If 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:

▪ Immediately after towel drying • At least every 2 hours • Sun Protection

Measures. Spending time in the sun increases your risk of skin cancer

and early skin aging. To decrease this risk, regularly use a sunscreen with

a broad spectrum SPF of 15 or higher and other sun protection measures

including: ▪ Limit time in sun, especially from 10 a.m.- 2 p.m.

▪ Wear long-sleeve shirts, pants, hats, and sunglasses ▪ Children under

6 months: Ask a doctor

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Ethylhexyl Palmitate, Silica, Caprylic/Capric, Triglyceride, Triisotridecyl Trimellitate, C12-15 Alkyl Benzoate, ydrogenated Microcrystalline Wax, HDI/Trimethylol Hexyllactone Crosspolymer, Aluminum Starch Octenylsuccinate, Polyethylene,

Ozokerite, Synthetic Wax, Hydroxycapric Acid, Hydroxycaprylic Acid, Hydroxycinnamic Acid, Teprenone, Butylene Glycol, Dimethicone,

Hydrogen Dimethicone, Kaolin, Mica, PEG-4, Synthetic Fluorphlogopite, Tin Oxide, Phenxoyethanol. May Contain: Blue 1

Lake, Iron Oxides, Red 40 Lake, Titanium Dioxide, Yellow 5 Lake

Other information

SPL UNCLASSIFIED SECTION

▪ Protect this product from excessive heat and direct sun

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package LabelPackage Label

Products#

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

DailyMed product names page 1 of 1 · 33 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70227-00170227-001-47, 70227-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 31 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
2575f3b6-ebca-1395-e054-00144ff8d46c2575f3b6-ebc9-1395-e054-00144ff8d46c2016-01-08WarningsExact identifier
spl id: 2575f3b6-ebca-1395-e054-00144ff8d46c
spl set id: 2575f3b6-ebc9-1395-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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