control corrective intensive skin brightening spf-30 sunscreen

Generic: octinoxate, octisalate, zinc oxide

Labeler: control corrective skincare inc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name control corrective intensive skin brightening spf-30 sunscreen
Generic Name octinoxate, octisalate, zinc oxide
Labeler control corrective skincare inc
Dosage Form CREAM
Routes
TOPICAL
Active Ingredients

octinoxate 6.9 g/100mL, octisalate 3 g/100mL, zinc oxide 4 g/100mL

Manufacturer
CONTROL CORRECTIVE SKINCARE INC

Identifiers & Regulatory

Product NDC 70764-205
Product ID 70764-205_474c2437-79fd-f67a-e063-6294a90a8060
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2018-09-11

Pharmacologic Class

Classes
copper absorption inhibitor [epc] decreased copper ion absorption [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70764205
Hyphenated Format 70764-205

Supplemental Identifiers

UNII
4Y5P7MUD51 4X49Y0596W SOI2LOH54Z

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name control corrective intensive skin brightening spf-30 sunscreen (source: ndc)
Generic Name octinoxate, octisalate, zinc oxide (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 6.9 g/100mL
  • 3 g/100mL
  • 4 g/100mL
source: ndc
Packaging
  • 1 TUBE in 1 BOX (70764-205-52) / 74 mL in 1 TUBE (70764-205-22)
source: ndc

Packages (1)

70764-205-52 1 TUBE in 1 BOX (70764-205-52) / 74 mL in 1 TUBE (70764-205-22)

Ingredients (3)

octinoxate (6.9 g/100mL) octisalate (3 g/100mL) zinc oxide (4 g/100mL)

Linked Drug Pages (1)

CONTROL CORRECTIVE INTENSIVE SKIN BRIGHTENING SPF-30 SUNSCREEN ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "474c2437-79fd-f67a-e063-6294a90a8060", "openfda": {"unii": ["4Y5P7MUD51", "4X49Y0596W", "SOI2LOH54Z"], "spl_set_id": ["61b6dab9-3378-4206-bf1f-6f385a9c882c"], "manufacturer_name": ["CONTROL CORRECTIVE SKINCARE INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 BOX (70764-205-52)  / 74 mL in 1 TUBE (70764-205-22)", "package_ndc": "70764-205-52", "marketing_start_date": "20180911"}], "brand_name": "CONTROL CORRECTIVE INTENSIVE SKIN BRIGHTENING SPF-30 SUNSCREEN", "product_id": "70764-205_474c2437-79fd-f67a-e063-6294a90a8060", "dosage_form": "CREAM", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "70764-205", "generic_name": "OCTINOXATE, OCTISALATE, ZINC OXIDE", "labeler_name": "CONTROL CORRECTIVE SKINCARE INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "CONTROL CORRECTIVE INTENSIVE SKIN BRIGHTENING", "brand_name_suffix": "SPF-30 SUNSCREEN", "active_ingredients": [{"name": "OCTINOXATE", "strength": "6.9 g/100mL"}, {"name": "OCTISALATE", "strength": "3 g/100mL"}, {"name": "ZINC OXIDE", "strength": "4 g/100mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180911", "listing_expiration_date": "20261231"}