PLAY Sunscreen SPF 50

UNIISPL

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

Identification

ManufacturerSupergoop LLC

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
7593664901
40 g in 1 TUBE (75936-649-01)

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": {
    "0428eebc-4ffb-4981-b738-2c9ecf2a6a2e": {
      "match": "brand_token",
      "title": "PLAY EVERYDAY FACE SPF 50 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE) LOTION [SUPERGOOP, LLC]",
      "spl_version": "8",
      "published_date": "2026-02-06"
    }
  },
  "productid": "75936-649_47fcc2bb-733f-34dc-e063-6394a90ac7ad",
  "productndc": "75936-649",
  "dosage_form": "STICK",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE",
  "proprietary_name": "PLAY Sunscreen SPF 50",
  "active_ingred_unit": "g/100g; g/100g; g/100g; g/100g",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Homosalate, Octocrylene, Octisalate, Avobenzone",
  "start_marketing_date": "20241203",
  "active_numerator_strength": "3; 7; 5; 7"
}

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