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United States · US · US:84423-046_29726662-5b38-d884-e063-6294a90a1f26
DARKSPOTREMOVERILLUMINATINGFACECREAM
UNIISPLATC A11GA
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerGuangzhou Kadiya Biotechnology Co., Ltd.
CountryUS (United States)
ATC codeA11GA
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11844230460130 mL in 1 BOTTLE, GLASS (84423-046-01)
Annotations
UNII (FDA Substance ID)
72VUP07IT5
ALPHA-ARBUTIN
RxCUI 1363429
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "72VUP07IT5",
"rxcui": "1363429",
"inchikey": "BJRNKVDFDLYUGJ-ZIQFBCGOSA-N",
"display_name": "ALPHA-ARBUTIN",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "CUTANEOUS",
"spl_meta": {
"29726662-5b37-d884-e063-6294a90a1f26": {
"match": "brand_token",
"title": "DARKSPOTREMOVERILLUMINATINGFACECREAM EMULSION [GUANGZHOU KADIYA BIOTECHNOLOGY CO., LTD.]",
"spl_version": "1",
"published_date": "2025-02-27"
}
},
"productid": "84423-046_29726662-5b38-d884-e063-6294a90a1f26",
"productndc": "84423-046",
"dosage_form": "EMULSION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ALPHA-ARBUTIN; ASCORBIC ACID; TOCOPHEROL",
"proprietary_name": "DARKSPOTREMOVERILLUMINATINGFACECREAM",
"active_ingred_unit": "g/30mL; g/30mL; g/30mL",
"application_number": "M016",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "DarkSpotRemoverIlluminatingFaceCream",
"start_marketing_date": "20241217",
"active_numerator_strength": ".3; .03; .015"
}Related drugs
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