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United States · US · US:70764-205_474c2437-79fd-f67a-e063-6294a90a8060
CONTROL CORRECTIVE INTENSIVE SKIN BRIGHTENING
UNIISPLATC D02BA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerCONTROL CORRECTIVE SKINCARE INC
CountryUS (United States)
ATC codeD02BA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1170764205521 TUBE in 1 BOX (70764-205-52) / 74 mL in 1 TUBE (70764-205-22)
Annotations
UNII (FDA Substance ID)
4Y5P7MUD51
OCTINOXATE
RxCUI 13369
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "4Y5P7MUD51",
"rxcui": "13369",
"inchikey": "YBGZDTIWKVFICR-JLHYYAGUSA-N",
"display_name": "OCTINOXATE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"61b6dab9-3378-4206-bf1f-6f385a9c882c": {
"match": "brand_token",
"title": "CONTROL CORRECTIVE INTENSIVE SKIN BRIGHTENING SPF-30 SUNSCREEN (OCTINOXATE, OCTISALATE, ZINC OXIDE) CREAM [CONTROL CORRECTIVE SKINCARE INC]",
"spl_version": "5",
"published_date": "2026-01-02"
}
},
"productid": "70764-205_474c2437-79fd-f67a-e063-6294a90a8060",
"productndc": "70764-205",
"dosage_form": "CREAM",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "OCTINOXATE; OCTISALATE; ZINC OXIDE",
"proprietary_name": "CONTROL CORRECTIVE INTENSIVE SKIN BRIGHTENING",
"active_ingred_unit": "g/100mL; g/100mL; g/100mL",
"application_number": "M020",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "OCTINOXATE, OCTISALATE, ZINC OXIDE",
"start_marketing_date": "20180911",
"active_numerator_strength": "6.9; 3; 4"
}Related drugs
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