🇺🇸
United States · US · US:49967-895_1cb9aca2-b493-4ee2-85c9-0001329654fc
Kiehls Since 1851 Dermatologist Solutions Breakout Control Targeted Acne Spot Treatment
UNIISPLATC D10AB02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerL'Oreal USA Products Inc
CountryUS (United States)
ATC codeD10AB02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 4
- ndc1149967895011 TUBE in 1 CARTON (49967-895-01) / 20 mL in 1 TUBE
- ndc1149967895023 mL in 1 PACKET (49967-895-02)
- ndc1149967895031.5 mL in 1 PACKET (49967-895-03)
- ndc1149967895043 mL in 1 TUBE (49967-895-04)
Annotations
UNII (FDA Substance ID)
70FD1KFU70
SULFUR
RxCUI 10223
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "70FD1KFU70",
"rxcui": "10223",
"inchikey": "JLQNHALFVCURHW-UHFFFAOYSA-N",
"display_name": "SULFUR",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"22e088b9-b3b1-4c34-be12-a5a31200ec25": {
"match": "brand_token",
"title": "KIEHLS SINCE 1851 ULTRA FACIAL MELTDOWN RECOVERY (COLLOIDAL OATMEAL) CREAM [L’OREAL USA PRODUCTS INC]",
"spl_version": "8",
"published_date": "2026-06-01"
}
},
"productid": "49967-895_1cb9aca2-b493-4ee2-85c9-0001329654fc",
"productndc": "49967-895",
"dosage_form": "LOTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "SULFUR",
"proprietary_name": "Kiehls Since 1851 Dermatologist Solutions Breakout Control Targeted Acne Spot Treatment",
"active_ingred_unit": "mg/mL",
"application_number": "M006",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Sulfur",
"start_marketing_date": "20161101",
"active_numerator_strength": "100"
}Related drugs
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