SEKKISEI HERBAL UV DEFENSE gel

UNIISPL

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

Identification

ManufacturerKOS� America, Inc.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 2

ndc11
6682004001
1 TUBE in 1 CARTON (66820-0400-1) / 30 mL in 1 TUBE
ndc11
6682004002
2 mL in 1 PACKET (66820-0400-2)

Annotations

UNII (FDA Substance ID)

G63QQF2NOX

AVOBENZONE

RxCUI 45045

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "G63QQF2NOX",
    "rxcui": "45045",
    "inchikey": "XNEFYCZVKIDDMS-UHFFFAOYSA-N",
    "display_name": "AVOBENZONE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "cb0faa3a-68f8-49c5-8c28-3338b1b27cd8": {
      "match": "brand_token",
      "title": "SEKKISEI HERBAL UV DEFENSE GEL (AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE) GEL [KOS&EACUTE; AMERICA, INC.]",
      "spl_version": "3",
      "published_date": "2026-01-05"
    }
  },
  "productid": "66820-0400_42ff269f-2905-3c40-e063-6394a90a323d",
  "productndc": "66820-0400",
  "dosage_form": "GEL",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE",
  "proprietary_name": "SEKKISEI HERBAL UV DEFENSE gel",
  "active_ingred_unit": "mg/mL; mg/mL; mg/mL; mg/mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "AVOBENZONE, HOMOSALATE, OCTISALATE, AND OCTOCRYLENE",
  "start_marketing_date": "20240301",
  "active_numerator_strength": "30; 95; 50; 26"
}

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