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United States · US · US:11822-1002_6c4b2dd2-0897-4bcb-a570-6bc6f5332828

all day allergy

Orange BookUNIISPLATC R06AE

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

Identification

ManufacturerRite Aid Corporation
CountryUS (United States)
ATC codeR06AE
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 6

  • ndc11
    1182210021
    14 BLISTER PACK in 1 CARTON (11822-1002-1) / 1 TABLET, FILM COATED in 1 BLISTER PACK
  • ndc11
    1182210022
    1 BOTTLE in 1 CARTON (11822-1002-2) / 30 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    1182210023
    1 BOTTLE in 1 CARTON (11822-1002-3) / 60 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    1182210024
    1 BOTTLE in 1 CARTON (11822-1002-4) / 120 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    1182210027
    1 BOTTLE in 1 CARTON (11822-1002-7) / 300 TABLET, FILM COATED in 1 BOTTLE
  • ndc11
    1182210028
    1 BOTTLE in 1 CARTON (11822-1002-8) / 90 TABLET, FILM COATED in 1 BOTTLE

Annotations

UNII (FDA Substance ID)
64O047KTOA
CETIRIZINE HYDROCHLORIDE
RxCUI 203150
Orange Book
A078336
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": {
    "8889af37-8345-4358-994d-7d8b847f4874": {
      "match": "brand_token",
      "title": "ALL DAY ALLERGY (CETIRIZINE HYDROCHLORIDE) TABLET, FILM COATED [HYVEE INC]",
      "spl_version": "6",
      "published_date": "2026-05-13"
    }
  },
  "productid": "11822-1002_6c4b2dd2-0897-4bcb-a570-6bc6f5332828",
  "productndc": "11822-1002",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "078336",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "5MG",
        "product_no": "001",
        "approval_date": "Dec 27, 2007"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "10MG",
        "product_no": "002",
        "approval_date": "Dec 27, 2007"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "5MG",
        "product_no": "003",
        "approval_date": "Dec 27, 2007"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "10MG",
        "product_no": "004",
        "approval_date": "Dec 27, 2007"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "CETIRIZINE HYDROCHLORIDE",
  "proprietary_name": "all day allergy",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA078336",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Cetirizine Hydrochloride",
  "start_marketing_date": "20210914",
  "active_numerator_strength": "10"
}

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