SUNSCREEN GLOWING, SPF 30

UNIISPL

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

Identification

ManufacturerFSA Store Inc

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
8152222001
50 mL in 1 BOTTLE (81522-220-01)

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": {
    "1cb7fbca-0874-ae53-e063-6294a90ab42a": {
      "match": "brand_token",
      "title": "SUNSCREEN FOR BABY SPF50PLUS (OCTOCRYLENE,ETHYLHEXYL METHOXYCINNAMATE,TITANIUM DIOXIDE,ETHYLHEXYL SALICYLATE) LOTION [GUANGZHOU SENMAI BIOTECHNOLOGY CO., LTD.]",
      "spl_version": "7",
      "published_date": "2026-04-03"
    }
  },
  "productid": "81522-220_473bcb90-ab80-170b-e063-6294a90a99d5",
  "productndc": "81522-220",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE",
  "proprietary_name": "SUNSCREEN GLOWING, SPF 30",
  "active_ingred_unit": "g/50mL; g/50mL; g/50mL; g/50mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "sunscreen glowing lotion",
  "start_marketing_date": "20251201",
  "active_numerator_strength": "1.5; 4.5; 2.5; 3.5"
}

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