Derma Pain

UNIISPL

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerLiddell Laboratories, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
5084502801
30 mL in 1 BOTTLE, SPRAY (50845-0280-1)

Annotations

UNII (FDA Substance ID)

18E7415PXQ

CALENDULA OFFICINALIS FLOWERING TOP

RxCUI 1309775

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "18E7415PXQ",
    "rxcui": "1309775",
    "inchikey": null,
    "display_name": "CALENDULA OFFICINALIS FLOWERING TOP",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "ba38a43d-7a8a-4814-ba34-0e99124f5fca": {
      "match": "brand_token",
      "title": "DERMA B EVERYDAY FIT SUNSCREEN SPF 50 (AVOBEZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [NEOPHARM CO., LTD.]",
      "spl_version": "2",
      "published_date": "2026-02-06"
    }
  },
  "productid": "50845-0280_f378a799-7c5f-45bf-a78b-1f9617f30121",
  "productndc": "50845-0280",
  "dosage_form": "SPRAY",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "CALENDULA OFFICINALIS FLOWERING TOP; CROTON TIGLIUM SEED; PLANTAGO MAJOR WHOLE; SMILAX ORNATA ROOT; SODIUM CHLORIDE; TOXICODENDRON PUBESCENS LEAF",
  "proprietary_name": "Derma Pain",
  "active_ingred_unit": "[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Calendula Officinalis, Croton Tiglium, Natrum Muriaticum, Plantago Major, Rhus Tox, Sarsaparilla (Smilax Regelii)",
  "start_marketing_date": "20220629",
  "active_numerator_strength": "12; 30; 30; 30; 30; 30"
}

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