Hand Sanitizer

NDC product · U.S. Food and Drug Administration (openFDA) · United States

Product NDC 59779-059
Package NDC 59779-059-34
Application number 505G(a)(3)
SPL ID 49ecc619-1d9e-e6a0-e063-6394a90a975d
SPL set ID 3ea2f838-3ad8-4913-8736-9da82f5cef4b
UNII 3K9958V90M
RxCUI 581662

What the source publishes

Labeler: CVS Pharmacy, Inc.
Active ingredients: Alcohol
Form: GEL
Routes: TOPICAL
Administrative status: present-in-source-snapshot
Marketing status: OTC MONOGRAPH DRUG
Product type: HUMAN OTC DRUG
Prescription: Non-prescription

Names this record is found by

Complete source data

us:fda:ndc:59779-059_49ecc619-1d9e-e6a0-e063-6394a90a975d

{
  "name": "Hand Sanitizer",
  "splId": "49ecc619-1d9e-e6a0-e063-6394a90a975d",
  "labels": [
    {
      "setId": "3ea2f838-3ad8-4913-8736-9da82f5cef4b",
      "labelUrl": "https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=3ea2f838-3ad8-4913-8736-9da82f5cef4b",
      "labelPdfUrl": "https://dailymed.nlm.nih.gov/dailymed/downloadpdffile.cfm?setId=3ea2f838-3ad8-4913-8736-9da82f5cef4b"
    }
  ],
  "routes": [
    "TOPICAL"
  ],
  "labeler": "CVS Pharmacy, Inc.",
  "finished": true,
  "packaging": [
    {
      "sample": false,
      "description": "236 mL in 1 BOTTLE, PUMP (59779-059-34)",
      "package_ndc": "59779-059-34",
      "identifierStatus": "well-formed",
      "marketing_start_date": "20130313"
    }
  ],
  "productId": "59779-059_49ecc619-1d9e-e6a0-e063-6394a90a975d",
  "useDomain": "unknown",
  "dosageForm": "GEL",
  "productNdc": "59779-059",
  "deaSchedule": null,
  "genericName": "Alcohol",
  "productType": "HUMAN OTC DRUG",
  "listingStatus": "present-in-source-snapshot",
  "targetSpecies": [],
  "approvalStatus": "not-established-by-ndc-listing",
  "labelAssociation": "openFDA-harmonized-set-ids; not a product-level approval match",
  "marketingEndDate": null,
  "activeIngredients": [
    {
      "name": "ALCOHOL",
      "strength": "70 mL/100mL"
    }
  ],
  "applicationNumber": "505G(a)(3)",
  "marketingCategory": "OTC MONOGRAPH DRUG",
  "stateRestrictions": {
    "status": "not-collected",
    "observations": []
  },
  "useDomainEvidence": {
    "basis": "unreviewed",
    "field": null,
    "value": null,
    "version": 1,
    "sourceId": "us.fda.ndc"
  },
  "marketingStartDate": "20130313",
  "targetSpeciesStatus": "not-reported",
  "prescriptionCategory": "non-prescription",
  "harmonizedIdentifiers": {
    "unii": [
      "3K9958V90M"
    ],
    "rxcui": [
      "581662"
    ],
    "spl_set_id": [
      "3ea2f838-3ad8-4913-8736-9da82f5cef4b"
    ],
    "manufacturer_name": [
      "CVS Pharmacy, Inc."
    ],
    "is_original_packager": [
      true
    ]
  },
  "listingExpirationDate": "20271231"
}

NDC Directory

U.S. Food and Drug Administration / openFDA

Retrieved: November 12, 2026
Licence: CC0 1.0
Source id: us.fda.ndc

Official source

What this source does not establish

Complete published endpoint, not a claim that FDA lists every medicine used in the US.
NDC listing, marketing category and application-number assertions are not proof of approval.
Tentative approval, discontinued products and historical submissions remain distinct.
Official document links only; linked documents have not been relicensed or mirrored.
No state restrictions, individual eligibility, or prescribing recommendations inferred.
UNII and RxNorm identifiers are source-asserted openFDA harmonization at record scope; arrays do not pair identifiers to individual products or ingredients, and are not GSID/PhPID or substitution evidence.

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