SPF 50 Sunscreen

UNIISPL

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

Identification

ManufacturerDerma Care Research Labs, LLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 3

ndc11
7283915902
59 mL in 1 BOTTLE, PLASTIC (72839-159-02)
ndc11
7283915906
177 mL in 1 BOTTLE, PLASTIC (72839-159-06)
ndc11
7283915932
946 mL in 1 BOTTLE, PUMP (72839-159-32)

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": {
    "e97d82fe-cd45-43a5-9c1f-3900025240a1": {
      "match": "brand_token",
      "title": "SPF 50 MINERAL SUNSCREEN FACE AND BODY (ZINC OXIDE) LOTION [TODDLE BORN WILD, INC.]",
      "spl_version": "3",
      "published_date": "2026-05-28"
    }
  },
  "productid": "72839-159_29a578a8-e2e2-a79d-e063-6294a90aa2a6",
  "productndc": "72839-159",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "AVOBENZONE; HOMOSALATE; OCTOCRYLENE",
  "proprietary_name": "SPF 50 Sunscreen",
  "active_ingred_unit": "g/100mL; g/100mL; g/100mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Avobenzone 3%, Homosalate 10%, Octocrylene 6%",
  "start_marketing_date": "20200327",
  "active_numerator_strength": "3; 10; 6"
}

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