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United States · US · US:42961-120_698cf169-c537-491e-9e70-b920b627761e

First Aid Direct Allergy Relief

Orange BookUNIISPLATC R06AX13

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

Identification

ManufacturerCintas Corporation
CountryUS (United States)
ATC codeR06AX13
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    4296112002
    2 BLISTER PACK in 1 BOX (42961-120-02) / 10 TABLET in 1 BLISTER PACK

Annotations

UNII (FDA Substance ID)
7AJO3BO7QN
LORATADINE
RxCUI 28889
Orange Book
A210722
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": {
    "5258cef2-0e5c-4ccd-e063-6394a90a9e5c": {
      "match": "brand_token",
      "title": "FIRST AID ONLY LIDOCAINE HYDROCHLORIDE ANALGESIC BURN GEL (LIDOCAINE HYDROCHLORIDE) GEL [ACME UNITED CORPORATION]",
      "spl_version": "1",
      "published_date": "2026-06-02"
    }
  },
  "productid": "42961-120_698cf169-c537-491e-9e70-b920b627761e",
  "productndc": "42961-120",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "210722",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "10MG",
        "product_no": "001",
        "approval_date": "Dec 23, 2019"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "LORATADINE",
  "proprietary_name": "First Aid Direct Allergy Relief",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA210722",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Loratadine Tablets",
  "start_marketing_date": "20211020",
  "active_numerator_strength": "10"
}

Related drugs

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