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United States · US · US:10237-731_38d791e8-33d3-22e4-e063-6394a90aff90

Orajel Rescue Relief Pen

UNIISPLATC C05AD

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

Identification

ManufacturerChurch & Dwight Co., Inc.
CountryUS (United States)
ATC codeC05AD
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 2

  • ndc11
    1023773107
    1 APPLICATOR in 1 BLISTER PACK (10237-731-07) / 2 g in 1 APPLICATOR
  • ndc11
    1023773127
    2 BLISTER PACK in 1 PACKAGE (10237-731-27) / 1 APPLICATOR in 1 BLISTER PACK / 2 g in 1 APPLICATOR

Annotations

UNII (FDA Substance ID)
U3RSY48JW5
BENZOCAINE
RxCUI 1399
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "U3RSY48JW5",
    "rxcui": "1399",
    "inchikey": "BLFLLBZGZJTVJG-UHFFFAOYSA-N",
    "display_name": "BENZOCAINE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "ce40829e-941f-2548-e053-2995a90a1e0e": {
      "match": "brand_token",
      "title": "ORAJEL COLD SORE TOUCH FREE - SINGLE DOSE (BENZALKONIUM CHLORIDE, BENZOCAINE) LIQUID [CHURCH & DWIGHT CO., INC.]",
      "spl_version": "6",
      "published_date": "2026-05-15"
    }
  },
  "productid": "10237-731_38d791e8-33d3-22e4-e063-6394a90aff90",
  "productndc": "10237-731",
  "dosage_form": "GEL",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "BENZOCAINE; MENTHOL; ZINC CHLORIDE",
  "proprietary_name": "Orajel Rescue Relief Pen",
  "active_ingred_unit": "mg/g; mg/g; mg/g",
  "application_number": "M022",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Oral Pain Reliever",
  "start_marketing_date": "20250201",
  "active_numerator_strength": "200; 2.6; 1.5"
}

Related drugs

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