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United States · US · US:37808-506_17e2e605-d5de-4d95-b5c8-710e56b61334

Childrens Allergy Relief

Orange BookUNIISPLATC R06AX13

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

Identification

ManufacturerH E B
CountryUS (United States)
ATC codeR06AX13
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 2

  • ndc11
    3780850639
    30 BLISTER PACK in 1 CARTON (37808-506-39) / 1 TABLET, CHEWABLE in 1 BLISTER PACK
  • ndc11
    3780850652
    10 BLISTER PACK in 1 CARTON (37808-506-52) / 1 TABLET, CHEWABLE in 1 BLISTER PACK

Annotations

UNII (FDA Substance ID)
7AJO3BO7QN
LORATADINE
RxCUI 28889
Orange Book
A210033
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": {
    "436c0126-4ff3-c082-e063-6294a90a3d72": {
      "match": "brand_token",
      "title": "CHILDRENS IBUPROFEN (IBUPROFEN) SUSPENSION [KESIN PHARMA CORPORATION]",
      "spl_version": "2",
      "published_date": "2026-06-01"
    }
  },
  "productid": "37808-506_17e2e605-d5de-4d95-b5c8-710e56b61334",
  "productndc": "37808-506",
  "dosage_form": "TABLET, CHEWABLE",
  "orange_book": {
    "appl_no": "210033",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "5MG",
        "product_no": "001",
        "approval_date": "Jun 12, 2019"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "LORATADINE",
  "proprietary_name": "Childrens Allergy Relief",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA210033",
  "marketing_category": "ANDA",
  "nonproprietary_name": "loratadine",
  "start_marketing_date": "20210819",
  "active_numerator_strength": "5"
}

Related drugs

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