Sunscreen SPF 50

UNIISPL

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

Identification

ManufacturerRocky Mountain

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 3

ndc11
4975701009
453 g in 1 BOTTLE (49757-010-09)
ndc11
4975701012
907 g in 1 CONTAINER (49757-010-12)
ndc11
4975701022
3629 g in 1 CONTAINER (49757-010-22)

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": "49757-010_4d4f240d-5656-cc29-e063-6294a90a7903",
  "productndc": "49757-010",
  "dosage_form": "SPRAY",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "AVOBENZONE; HOMOSALATE; OCTISALATE",
  "proprietary_name": "Sunscreen SPF 50",
  "active_ingred_unit": "g/100g; g/100g; g/100g",
  "application_number": "M20",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Avobenzone 3% , Homosalate 10%,Octisalate 5%",
  "start_marketing_date": "20250821",
  "active_numerator_strength": "3; 10; 5"
}

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