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United States · US · US:79481-0981_8d69bdb3-957b-4af3-9255-79dda46dd5fd

24 hour allergy

Orange BookUNIISPLATC R06AE

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

Identification

ManufacturerMeijer, Inc.
CountryUS (United States)
ATC codeR06AE
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    7948109810
    1 BOTTLE in 1 PACKAGE (79481-0981-0) / 25 CAPSULE, LIQUID FILLED in 1 BOTTLE

Annotations

UNII (FDA Substance ID)
64O047KTOA
CETIRIZINE HYDROCHLORIDE
RxCUI 203150
Orange Book
A213105
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "64O047KTOA",
    "rxcui": "203150",
    "inchikey": "PGLIUCLTXOYQMV-UHFFFAOYSA-N",
    "display_name": "CETIRIZINE HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "53ca807b-3ec2-4b5e-aa5a-6dcb756bb423": {
      "match": "brand_token",
      "title": "24 7 RELIEF AND RECOVERY PAIN RELIEVING (MENTHOL, UNSPECIFIED FORM) CREAM [TRIPLICARE INC]",
      "spl_version": "1",
      "published_date": "2026-05-06"
    }
  },
  "productid": "79481-0981_8d69bdb3-957b-4af3-9255-79dda46dd5fd",
  "productndc": "79481-0981",
  "dosage_form": "CAPSULE, LIQUID FILLED",
  "orange_book": {
    "appl_no": "213105",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "10MG",
        "product_no": "001",
        "approval_date": "Sep 21, 2020"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "CETIRIZINE HYDROCHLORIDE",
  "proprietary_name": "24 hour allergy",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA213105",
  "marketing_category": "ANDA",
  "nonproprietary_name": "cetirizine hydrochloride",
  "start_marketing_date": "20220308",
  "active_numerator_strength": "10"
}

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