FDA.reportPublic FDA data

CONTROL CORRECTIVE INTENSIVE SKIN BRIGHTENING CREAM SPF 30 SUNSCREEN (70764-205)

Manufacturer
CONTROL CORRECTIVE SKINCARE INC | Chemolee Lab Corporation
Effective date
2025-12-31
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:30:17

Label at a glance#

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

Dosage and administration

MAY BE USED TWICE DAILY WHEN APPLIED TO CLEAN, DRY 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 , NON-GREASY MOISTURIZER AND SUNSCREEN TO HELP REDUCE FREE RADICAL DAMAGE AND ENCOURAGE SKIN BRIGHTENING.

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

MAY BE USED TWICE DAILY WHEN APPLIED TO CLEAN, DRY 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, KOJIC DIPALMITATE, CETEARYL ALCOHOL, CETEARETH-20, VP/EICOSENE COPOLYMER, HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER, SQUALANE, POLYSORBATE 60, CYCLOTETRASILOXANE, ARCTOSTAPHYLOS UVA URSI LEAF EXTRACT, GLYCYRRHIZA GLABRA ROOT EXTRACT, PHENOXYETHANOL, BUTYROSPERMUM PARKII SHEA BUTTER, PERSEA GRATISSIMA OIL, FRAGRANCE, TOCOPHERYL ACETATE, DISODIUM EDTA, TRIETHOXYCAPRYLYLSILANE, ARBUTIN, CITRIC ACID, 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

Box IntensiveSkinBrightening CreamCarton-new2-olLBox IntensiveSkinBrightening CreamCarton-new2-olL

DailyMed Pharmacologic Classes#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f47a510b-6679-4664-b2d6-47b5c4afe7ccProduct name420260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70764-205-522025-12-31C16284748780-12cef2736-9481-d83d-e063-dadaa90ab31fCONTROL CORRECTIVE INTENSIVE SKIN BRIGHTENING CREAM SPF 30 SUNSCREEN (70764-205)
70764-205-522025-01-30C16284748780-12cef2736-9481-d83d-e063-dadaa90ab31fCONTROL CORRECTIVE INTENSIVE SKIN BRIGHTENING CREAM SPF 30 SUNSCREEN (70764-205)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70764-205-22CONTROL CORRECTIVE INTENSIVE SKIN BRIGHTENINGSPF-30 SUNSCREEN74 mL in 1 TUBECREAM745
70764-205-52CONTROL CORRECTIVE INTENSIVE SKIN BRIGHTENINGSPF-30 SUNSCREEN1 in 1 BOXCREAM15

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
70764-20570764-205-22, 70764-205-52

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 29 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALOE VERA LEAFZY81Z83H0XIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
ISOPROPYL PALMITATE8CRQ2TH63MIACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
CYCLOMETHICONE 50THT5PCI0RIACT
KOJIC DIPALMITATE13N249RWTMIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
POLYOXYL 20 CETOSTEARYL ETHERYRC528SWUYIACT
VINYLPYRROLIDONE/EICOSENE COPOLYMER035MV9S1C3IACT
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%)86FQE96TZ4IACT
SQUALANEGW89575KF9IACT
POLYSORBATE 60CAL22UVI4MIACT
CYCLOMETHICONE 4CZ227117JEIACT
ARCTOSTAPHYLOS UVA-URSI LEAF3M5V3D1X36IACT
GLYCYRRHIZA INFLATA ROOT1MV1Z7MKVQIACT
PHENOXYETHANOLHIE492ZZ3TIACT
SHEA BUTTERK49155WL9YIACT
AVOCADO OIL6VNO72PFC1IACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
EDETATE DISODIUM7FLD91C86KIACT
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT
ARBUTINC5INA23HXFIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
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 INTENSIVE SKIN BRIGHTENING SPF-30 SUNSCREENOCTINOXATE, OCTISALATE, ZINC OXIDECONTROL CORRECTIVE SKINCARE INC61b6dab9-3378-4206-bf1f-6f385a9c882c2025-12-31WarningsExact identifier
ndc (package): 70764-205-22
ndc (package): 70764-205-52
ndc (product): 70764-205
ndc11 (package): 70764020522
ndc11 (package): 70764020552
spl id: 474c2437-79fd-f67a-e063-6294a90a8060
spl set id: 61b6dab9-3378-4206-bf1f-6f385a9c882c

Reported adverse events (FAERS/openFDA)#

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