CONTROL CORRECTIVE SUNSCREEN

Product NDC
70764-204
11-digit product format
707640204
Labeler code
70764
Product ID
70764-204_474c0af1-db90-a31e-e063-6394a90af093
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

Additional Listing Data#

Finished product
Yes
Brand name base
CONTROL CORRECTIVE SUNSCREEN
Brand name suffix
SPF-30
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

FDA-Initiated Inactive NDC Indexing#

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

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70764-204CONTROL CORRECTIVE SUNSCREEN SPF-30 (OCTINOXATE, OCTISALATE, ZINC OXIDE) CREAM [CONTROL CORRECTIVE SKINCARE INC]8Current NDC, Legacy NDC, 2 package rows20230924_e389b2bc-bb1c-443a-9bf6-c6d96380f378.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70764-204-217076402042174 mL in 1 BOTTLE74 mlHistorical
70764-204-52707640204521 BOTTLE in 1 BOX (70764-204-52) / 74 mL in 1 BOTTLE (70764-204-21) 1 bottle2018-09-110000-00-00NoNoCurrent