SunBurnt Advanced After-Sun

UNIISPL

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

Identification

ManufacturerWelmedix LLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 2

ndc11
2433021003
1 TUBE in 1 CARTON (24330-210-03) / 71 g in 1 TUBE
ndc11
2433021006
1 TUBE in 1 CARTON (24330-210-06) / 170 g in 1 TUBE

Annotations

UNII (FDA Substance ID)

P0M7O4Y7YD

CALENDULA OFFICINALIS FLOWER

RxCUI 1309289

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "P0M7O4Y7YD",
    "rxcui": "1309289",
    "inchikey": null,
    "display_name": "CALENDULA OFFICINALIS FLOWER",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "12de2559-05b0-4580-84c1-d3bd010b1c99": {
      "match": "brand_token",
      "title": "SUNBURNT PLUS (LIDOCAINE HYDROCHLORIDE) GEL [QUEST PRODUCTS, LLC.]",
      "spl_version": "5",
      "published_date": "2026-02-20"
    }
  },
  "productid": "24330-210_3d715022-70be-44aa-bfa3-f37823e35421",
  "productndc": "24330-210",
  "dosage_form": "GEL",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "CALENDULA OFFICINALIS FLOWER; ECHINACEA ANGUSTIFOLIA; LYTTA VESICATORIA",
  "proprietary_name": "SunBurnt Advanced After-Sun",
  "active_ingred_unit": "[hp_Q]/.1g; [hp_Q]/.1g; [hp_X]/.1g",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "Calendula Officinalis, Echinacea Angustifolia, Cantharis Vesicatoria",
  "start_marketing_date": "20070101",
  "active_numerator_strength": "1; 1; 3"
}

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