EXTRA STRENGTH HUA TUO PAIN RELIEVING

UNIISPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerZhejiang Dingtai Pharmaceutical Co., Ltd

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
6907030701
1 POUCH in 1 BOX (69070-307-01) / 5 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": "69070-307_4345be21-4ba4-122d-e063-6394a90a5fa7",
  "productndc": "69070-307",
  "dosage_form": "PLASTER",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "CAMPHOR (SYNTHETIC); MENTHOL",
  "proprietary_name": "EXTRA STRENGTH HUA TUO PAIN RELIEVING",
  "active_ingred_unit": "g/100g; g/100g",
  "application_number": "M017",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Camphor and Menthol",
  "start_marketing_date": "20190409",
  "active_numerator_strength": "3.1; 2.6"
}

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