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United States · US · US:65923-532_425530d6-e8ea-f05c-e063-6294a90aff39
Coralite Ultra Strength Pain Relief
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerUnited Exchange Corp.
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1165923532181 JAR in 1 CARTON (65923-532-18) / 18 g in 1 JAR
Annotations
UNII (FDA Substance ID)
5TJD82A1ET
CAMPHOR (SYNTHETIC)
RxCUI 1371994
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "5TJD82A1ET",
"rxcui": "1371994",
"inchikey": "DSSYKIVIOFKYAU-XCBNKYQSSA-N;DSSYKIVIOFKYAU-OIBJUYFYSA-N",
"display_name": "CAMPHOR (SYNTHETIC)",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "TOPICAL",
"spl_meta": {
"ae314478-b8ab-4e90-bd0a-7a882d5c1b2e": {
"match": "brand_token",
"title": "CORALITE EXTRA STRENGTH PAIN RELIEF SLEEVE WRIST (MENTHOL) PATCH [UNITED EXCHANGE CORP.]",
"spl_version": "8",
"published_date": "2025-11-17"
}
},
"productid": "65923-532_425530d6-e8ea-f05c-e063-6294a90aff39",
"productndc": "65923-532",
"dosage_form": "OINTMENT",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "CAMPHOR (SYNTHETIC); MENTHOL",
"proprietary_name": "Coralite Ultra Strength Pain Relief",
"active_ingred_unit": "mg/g; mg/g",
"application_number": "M017",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Camphor Menthol",
"start_marketing_date": "20141015",
"active_numerator_strength": "110; 110"
}Access this data programmatically
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