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United States · US · US:83509-003_2c2dbdc7-8d2d-4ad3-e063-6294a90a6c7e

Bubble Fade Away Acne Spot Treatment

UNIISPLATC D10AE01

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerBUBBLE BEAUTY
CountryUS (United States)
ATC codeD10AE01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    8350900301
    1 TUBE in 1 CARTON (83509-003-01) / 10 mL in 1 TUBE

Annotations

UNII (FDA Substance ID)
W9WZN9A0GM
BENZOYL PEROXIDE
RxCUI 1418
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "W9WZN9A0GM",
    "rxcui": "1418",
    "inchikey": "OMPJBNCRMGITSC-UHFFFAOYSA-N",
    "display_name": "BENZOYL PEROXIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "d2eca90f-9463-4d2f-975d-02f2802ded3e": {
      "match": "brand_token",
      "title": "BUBBLE SOLAR MATE DAILY MINERAL SUNSCREEN SPF 40 (ZINC OXIDE) CREAM [BUBBLE BEAUTY, INC.]",
      "spl_version": "2",
      "published_date": "2026-05-28"
    }
  },
  "productid": "83509-003_2c2dbdc7-8d2d-4ad3-e063-6294a90a6c7e",
  "productndc": "83509-003",
  "dosage_form": "EMULSION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "BENZOYL PEROXIDE",
  "proprietary_name": "Bubble Fade Away Acne Spot Treatment",
  "active_ingred_unit": "mg/mL",
  "application_number": "M006",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Benzoyl Peroxide",
  "start_marketing_date": "20241201",
  "active_numerator_strength": "50"
}

Related drugs

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