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United States · US · US:72839-987_29b762dd-130b-def5-e063-6394a90a2b50
Outback Pain Relief
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerDerma Care Research Labs, LLC
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11728399870257 g in 1 TUBE (72839-987-02)
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": {
"c238c930-2012-2d48-e053-2a95a90a8a4a": {
"match": "brand_token",
"title": "OUTBACK PAIN RELIEF (CAMPHOR 6%, MENTHOL 16%) CREAM [DERMA CARE RESEARCH LABS, LLC]",
"spl_version": "3",
"published_date": "2024-12-23"
}
},
"productid": "72839-987_29b762dd-130b-def5-e063-6394a90a2b50",
"productndc": "72839-987",
"dosage_form": "CREAM",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "CAMPHOR (SYNTHETIC); MENTHOL",
"proprietary_name": "Outback Pain Relief",
"active_ingred_unit": "g/100g; g/100g",
"application_number": "M017",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "Camphor 6%, Menthol 16%",
"start_marketing_date": "20210513",
"active_numerator_strength": "6; 16"
}Access this data programmatically
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