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United States · US · US:11084-010_eb4c478c-f612-4163-9145-59d414bc8273

Refresh AntiBac FOAM

UNIISPLATC D08AJ01

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

Identification

ManufacturerSC Johnson Professional USA Inc.
CountryUS (United States)
ATC codeD08AJ01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 4

  • ndc11
    1108401005
    3.78 L in 1 BOTTLE, PLASTIC (11084-010-05)
  • ndc11
    1108401012
    1.2 L in 1 BOTTLE, PLASTIC (11084-010-12)
  • ndc11
    1108401020
    2 L in 1 BOTTLE, PLASTIC (11084-010-20)
  • ndc11
    1108401066
    1 L in 1 BOTTLE, PLASTIC (11084-010-66)

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": {
    "31bf1d6c-9719-4060-b6a3-409a2fe7b560": {
      "match": "brand_token",
      "title": "REFRESH CLASSIC (POLYVINYL ALCOHOL, POVIDONE) SOLUTION/ DROPS [ALLERGAN, INC.]",
      "spl_version": "11",
      "published_date": "2026-05-21"
    }
  },
  "productid": "11084-010_eb4c478c-f612-4163-9145-59d414bc8273",
  "productndc": "11084-010",
  "dosage_form": "SOAP",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "BENZALKONIUM CHLORIDE",
  "proprietary_name": "Refresh AntiBac FOAM",
  "active_ingred_unit": "g/L",
  "application_number": "505G(a)(3)",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Benzalkonium Chloride",
  "start_marketing_date": "20170612",
  "active_numerator_strength": ".13"
}

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