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United States · US · US:72476-004_50eb1e0e-2183-ec8d-e063-6294a90a34f5

Careone Amber

UNIISPLATC D08AJ01

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

Identification

ManufacturerRetail Business Services, LLC
CountryUS (United States)
ATC codeD08AJ01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 3

  • ndc11
    7247600402
    222 mL in 1 BOTTLE, PLASTIC (72476-004-02)
  • ndc11
    7247600403
    333 mL in 1 BOTTLE, PLASTIC (72476-004-03)
  • ndc11
    7247600404
    1660 mL in 1 BOTTLE, PLASTIC (72476-004-04)

Annotations

UNII (FDA Substance ID)
F5UM2KM3W7
BENZALKONIUM CHLORIDE
RxCUI 1379
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "F5UM2KM3W7",
    "rxcui": "1379",
    "inchikey": null,
    "display_name": "BENZALKONIUM CHLORIDE",
    "substance_type": "mixture",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "206f5483-7de1-4bc3-af27-190e211bcb95": {
      "match": "brand_token",
      "title": "CAREONE ACID RELIEF (FAMOTIDINE) TABLET, FILM COATED [AMERICAN SALES COMPANY]",
      "spl_version": "9",
      "published_date": "2026-05-25"
    }
  },
  "productid": "72476-004_50eb1e0e-2183-ec8d-e063-6294a90a34f5",
  "productndc": "72476-004",
  "dosage_form": "SOAP",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "BENZALKONIUM CHLORIDE",
  "proprietary_name": "Careone Amber",
  "active_ingred_unit": "mg/100mL",
  "application_number": "505G(a)(3)",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Benzalkonium Chloride",
  "start_marketing_date": "20210901",
  "active_numerator_strength": "130"
}

Related drugs

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