FDA.reportPublic FDA data

CONTROL CORRECTIVE SUNSCREEN

Manufacturer
CONTROL CORRECTIVE SKINCARE INC
Effective date
2025-12-31
Label type
HUMAN OTC DRUG LABEL
Version
9
Source
full-release
Hydrated at
2026-06-01 01:30:45

Label at a glance#

ProductCONTROL CORRECTIVE SUNSCREEN SPF-30
Active ingredientOCTINOXATE, OCTISALATE, ZINC OXIDE
Label structure10 sections

Dosage and administration

APPLY GENEROUSLY AND EVENLY TO SKIN 15 MINUTES PRIOR TO SUN EXPOSURE. IDEAL FOR ALL SKIN TYPES. PENETRATES QUICKLY AND LEAVES SKIN HYDRATED. SAFE FOR SENSITIVE SKIN.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

OCTINOXATE (6.9%)

OCTISALATE (3.0%)

ZINC OXIDE (4.0%)

PURPOSE

OTC - PURPOSE SECTION

SUNSCREEN

USE

INDICATIONS & USAGE SECTION

A MULTI-PURPOSE SUNSCREEN AND FACIAL MOISTURIZER. OFFERS BROAD SPECTRUM UVA & UVB PROTECTION WITHOUT LEAVING A GREASY FILM. HELPS PREVENT AGAINST TANNING AND BURNING. CONTAINS ALOE VERA AND ANTIOXIDANTS TO HELP SOOTHE AND BALANCE THE SKIN. MAY BE USED AS A FACIAL MOISTURIZER TO HELP FIGHT THE SIGNS OF AGING WHICH INCLUDES WRNKLING, DRYNESS, PIGMENTATION AND REDNESS.

WARNING

WARNINGS SECTION

FOR EXTERNAL USE ONLY. WHEN USING THIS PRODUCT, AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE THOROUGHLY WITH WATER. DISCONTINUE USE AND ASK A DOCTOR IF IRRITATION OR RASH DEVELOPS.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

APPLY GENEROUSLY AND EVENLY TO SKIN 15 MINUTES PRIOR TO SUN EXPOSURE. IDEAL FOR ALL SKIN TYPES. PENETRATES QUICKLY AND LEAVES SKIN HYDRATED. SAFE FOR SENSITIVE SKIN.

OTHER SAFETY INFORMATION

SUN ALERT: LIMITING SUN EXPOSURE, WEARING PROTECTIVE CLOTHING, AND USING SUNSCREEN MAY REDUCE THE RISK OF SKIN AGING, SKIN CANCER, AND OTHER HARMFUL EFFECTS OF THE SUN.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

WATER, ALOE BARBADENSIS LEAF, GLYCERIN, PROPYLENE GLYCOL, ISOPROPYL PALMITATE, CAPRYLIC/CAPRIC TRIGLYCERIDES, CYCLOPENTASILOXANE, CETEARYL ALCOHOL, CETEARETH-20, VP/EICOSENE COPOLYMER, HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER, SQUALANE, POLYSORBATE 60, ACANTHOPANAX SENTICOSUS (ELEUTHERO) ROOT EXTRACT, SYMPHYTUM OFFICINALE LEAF EXTRACT, CITRIC ACID, SODIUM HYALURONATE, CYCLOTETRASILOXANE, PHENOXYETHANOL, TOCOPHERYL ACETATE, TRIETHOXYCAPRYLYLSILANE, METHYLISOTHIAZOLINONE

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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b UC_Oil Free Sunscreen SPF 3001b UC_Oil Free Sunscreen SPF 30

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
ZINC CATION Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70764-204-522025-12-31C16284748780-12cef2736-8a43-d83d-e063-dadaa90ab31fCONTROL CORRECTIVE - OIL FREE SUNSCREEN SPF-30 (70764-204)
70764-204-522025-01-30C16284748780-12cef2736-8a43-d83d-e063-dadaa90ab31fCONTROL CORRECTIVE - OIL FREE SUNSCREEN SPF-30 (70764-204)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70764-204-21CONTROL CORRECTIVE SUNSCREENSPF-3074 mL in 1 BOTTLECREAM749
70764-204-52CONTROL CORRECTIVE SUNSCREENSPF-301 in 1 BOXCREAM19

Products#

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

DailyMed product names page 1 of 1 · 29 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70764-20470764-204-21, 70764-204-52

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 26 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
ISOPROPYL PALMITATE8CRQ2TH63MIACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
CYCLOMETHICONE 50THT5PCI0RIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
POLYOXYL 20 CETOSTEARYL ETHERYRC528SWUYIACT
VINYLPYRROLIDONE/EICOSENE COPOLYMER035MV9S1C3IACT
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%)86FQE96TZ4IACT
SQUALANEGW89575KF9IACT
POLYSORBATE 60CAL22UVI4MIACT
ELEUTHEROZQH6VH092ZIACT
COMFREY LEAFDG4F8T839XIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
HYALURONATE SODIUMYSE9PPT4THIACT
CYCLOMETHICONE 4CZ227117JEIACT
PHENOXYETHANOLHIE492ZZ3TIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
EDETATE DISODIUM7FLD91C86KIACT
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
OCTINOXATE4Y5P7MUD51ACTIB
OCTISALATE4X49Y0596WACTIB
ZINC OXIDESOI2LOH54ZACTIM

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
CONTROL CORRECTIVE SUNSCREEN SPF-30OCTINOXATE, OCTISALATE, ZINC OXIDECONTROL CORRECTIVE SKINCARE INCe389b2bc-bb1c-443a-9bf6-c6d96380f3782025-12-31WarningsExact identifier
ndc (package): 70764-204-52
ndc (package): 70764-204-21
ndc (product): 70764-204
ndc11 (package): 70764020421
ndc11 (package): 70764020452
spl id: 474c0af1-db90-a31e-e063-6394a90af093
spl set id: e389b2bc-bb1c-443a-9bf6-c6d96380f378

Reported adverse events (FAERS/openFDA)#

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