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United States · US · US:79903-156_eced88ce-e1bf-46d5-b523-d9e6142f03cc

All Day Allergy Relief

Orange BookUNIISPLATC R06AX13

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

Identification

ManufacturerWALMART INC. (see also Equate)
CountryUS (United States)
ATC codeR06AX13
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 5

  • ndc11
    7990315610
    10 BLISTER PACK in 1 CARTON (79903-156-10) / 1 TABLET in 1 BLISTER PACK
  • ndc11
    7990315612
    2 BOTTLE, PLASTIC in 1 BOX (79903-156-12) / 60 TABLET in 1 BOTTLE, PLASTIC
  • ndc11
    7990315645
    1 BOTTLE, PLASTIC in 1 BOX (79903-156-45) / 45 TABLET in 1 BOTTLE, PLASTIC
  • ndc11
    7990315660
    1 BOTTLE, PLASTIC in 1 BOX (79903-156-60) / 60 TABLET in 1 BOTTLE, PLASTIC
  • ndc11
    7990315699
    2 BOTTLE, PLASTIC in 1 BOX (79903-156-99) / 150 TABLET in 1 BOTTLE, PLASTIC

Annotations

UNII (FDA Substance ID)
7AJO3BO7QN
LORATADINE
RxCUI 28889
Orange Book
A075209
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "7AJO3BO7QN",
    "rxcui": "28889",
    "inchikey": "JCCNYMKQOSZNPW-UHFFFAOYSA-N",
    "display_name": "LORATADINE",
    "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": "79903-156_eced88ce-e1bf-46d5-b523-d9e6142f03cc",
  "productndc": "79903-156",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "075209",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "10MG",
        "product_no": "001",
        "approval_date": "Jan 21, 2003"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "LORATADINE",
  "proprietary_name": "All Day Allergy Relief",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA075209",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Loratadine",
  "start_marketing_date": "20221130",
  "active_numerator_strength": "10"
}

Related drugs

Other records sharing ATC code R06AX13.

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