FDA.reportPublic FDA data

CONTROL CORRECTIVE INTENSIVE SKIN BRIGHTENING

Product NDC
70764-205
11-digit product format
707640205
Labeler code
70764
Product ID
70764-205_474c2437-79fd-f67a-e063-6294a90a8060
Type
HUMAN OTC DRUG
Nonproprietary name
OCTINOXATE, OCTISALATE, ZINC OXIDE
Dosage form
CREAM
Route
TOPICAL
Labeler
CONTROL CORRECTIVE SKINCARE INC
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2018-09-11
Substance
OCTINOXATE; OCTISALATE; ZINC OXIDE
Active strength
6.9; 3; 4 g/100mL; g/100mL; g/100mL
Pharmacologic classes
Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report.

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

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

warnings

WARNING 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.

Additional Listing Data#

Finished product
Yes
Brand name base
CONTROL CORRECTIVE INTENSIVE SKIN BRIGHTENING
Brand name suffix
SPF-30 SUNSCREEN
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
OCTINOXATE6.9 g/100mL
OCTISALATE3 g/100mL
ZINC OXIDE4 g/100mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii4Y5P7MUD51, 4X49Y0596W, SOI2LOH54Z

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

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70764-205CONTROL CORRECTIVE INTENSIVE SKIN BRIGHTENING SPF-30 SUNSCREEN (OCTINOXATE, OCTISALATE, ZINC OXIDE) CREAM [CONTROL CORRECTIVE SKINCARE INC]4Current NDC, Legacy NDC, 2 package rows20230923_61b6dab9-3378-4206-bf1f-6f385a9c882c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70764-205-227076402052274 mL in 1 TUBE74 mlHistorical
70764-205-52707640205521 TUBE in 1 BOX (70764-205-52) / 74 mL in 1 TUBE (70764-205-22) 1 tube2018-09-110000-00-00NoNoCurrent