🇺🇸
United States · US · US:14222-2420_bbb80b31-6ecc-4d23-a2c3-784c6ea2289c
SOOTHE Sensitive Skin Treatment
UNIISPLATC P03AX
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerRodan & Fields
CountryUS (United States)
ATC codeP03AX
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 3
- ndc1114222242011 BOTTLE in 1 CARTON (14222-2420-1) / 50 mL in 1 BOTTLE
- ndc1114222242021 TUBE in 1 CARTON (14222-2420-2) / 10 mL in 1 TUBE
- ndc1114222242032 mL in 1 PACKET (14222-2420-3)
Annotations
UNII (FDA Substance ID)
344S277G0Z
ALLANTOIN
RxCUI 508
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "344S277G0Z",
"rxcui": "508",
"inchikey": "POJWUDADGALRAB-UHFFFAOYSA-N",
"display_name": "ALLANTOIN",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"450483c3-487f-4a8f-a439-5661241a8f0f": {
"match": "brand_token",
"title": "SOOTHE (BISMUTH SUBSALICYLATE) LIQUID [WALGREENS]",
"spl_version": "6",
"published_date": "2026-04-09"
}
},
"productid": "14222-2420_bbb80b31-6ecc-4d23-a2c3-784c6ea2289c",
"productndc": "14222-2420",
"dosage_form": "LOTION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ALLANTOIN; DIMETHICONE",
"proprietary_name": "SOOTHE Sensitive Skin Treatment",
"active_ingred_unit": "g/100mL; g/100mL",
"application_number": "M016",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Allantoin, Dimethicone",
"start_marketing_date": "20210309",
"active_numerator_strength": ".5; 2"
}Related drugs
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