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United States · US · US:55614-630_4346c26f-c1e0-1ac9-e063-6394a90a6a70
EXTRA STRENGTH HUA TUO PAIN RELIEF
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerMADISON ONE ACME INC
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1155614630011 POUCH in 1 BOX (55614-630-01) / 6 PATCH in 1 POUCH / 1 g in 1 PATCH
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": "TRANSDERMAL",
"spl_meta": {
"525467fb-510d-0b4b-e063-6294a90acd36": {
"match": "brand_token",
"title": "EXTRA STRENGTH TYLENOL COLD PLUS FLU MULTI-SYMPTOM NIGHTTIME (ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE) LIQUID [KENVUE BRANDS LLC]",
"spl_version": "1",
"published_date": "2026-06-02"
}
},
"productid": "55614-630_4346c26f-c1e0-1ac9-e063-6394a90a6a70",
"productndc": "55614-630",
"dosage_form": "PATCH",
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "CAMPHOR (SYNTHETIC); MENTHOL",
"proprietary_name": "EXTRA STRENGTH HUA TUO PAIN RELIEF",
"active_ingred_unit": "g/100g; g/100g",
"application_number": "M017",
"marketing_category": "OTC MONOGRAPH DRUG",
"nonproprietary_name": "CAMPHOR AND MENTHOL",
"start_marketing_date": "20200401",
"active_numerator_strength": "3.1; 2.6"
}Access this data programmatically
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