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United States · US · US:53125-801_40a72db6-d505-3e66-e063-6294a90a6566

North Woods Derma Gel Clear

UNIISPLATC D08AX08

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerSuperior Chemical Corporation
CountryUS (United States)
ATC codeD08AX08
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 3

  • ndc11
    5312580104
    3780 mL in 1 BOTTLE, PLASTIC (53125-801-04)
  • ndc11
    5312580129
    1000 mL in 1 BAG (53125-801-29)
  • ndc11
    5312580157
    550 mL in 1 BOTTLE, PUMP (53125-801-57)

Annotations

UNII (FDA Substance ID)
3K9958V90M
ALCOHOL
RxCUI 448
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "3K9958V90M",
    "rxcui": "448",
    "inchikey": "LFQSCWFLJHTTHZ-UHFFFAOYSA-N",
    "display_name": "ALCOHOL",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "068343b8-0435-40d0-846c-9d8624e8b6c4": {
      "match": "brand_token",
      "title": "NORTH STAR NUTRITIONALS SOOTHANOL X3 PAIN RELIEVING DROPS (MENTHOL) LIQUID [NEWMARKET HEALTH PRODUCTS, LLC]",
      "spl_version": "1",
      "published_date": "2026-05-22"
    }
  },
  "productid": "53125-801_40a72db6-d505-3e66-e063-6294a90a6566",
  "productndc": "53125-801",
  "dosage_form": "GEL",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ALCOHOL",
  "proprietary_name": "North Woods Derma Gel Clear",
  "active_ingred_unit": "mL/mL",
  "application_number": "505G(a)(3)",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Alcohol",
  "start_marketing_date": "20190801",
  "active_numerator_strength": ".7"
}

Related drugs

Other records sharing ATC code D08AX08.

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