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United States · US · US:76348-720_347e1804-127a-52a4-e063-6394a90ad676
DermaRad Relief
UNIISPLATC C01BB
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerRENU LABORATORIES, LLC
CountryUS (United States)
ATC codeC01BB
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1176348720011 TUBE in 1 BOX (76348-720-01) / 118 mL in 1 TUBE (76348-720-04)
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": {
"e5d64929-fb9c-7ebc-e053-2995a90a9318": {
"match": "brand_token",
"title": "DERMARAD RELIEF POST RADIATION CALMING (LIDOCAINE 3 PERCENT) LIQUID [RENU LABORATORIES, LLC]",
"spl_version": "2",
"published_date": "2025-05-12"
}
},
"productid": "76348-720_347e1804-127a-52a4-e063-6394a90ad676",
"productndc": "76348-720",
"dosage_form": "EMULSION",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "ALLANTOIN; LIDOCAINE",
"proprietary_name": "DermaRad Relief",
"active_ingred_unit": "g/118mL; g/118mL",
"application_number": "M017",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Lidocaine Emulsion",
"start_marketing_date": "20220103",
"active_numerator_strength": "1.18; 4.72"
}Related drugs
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