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United States · US · US:0299-4930_0a1d0295-47d8-41f4-aaeb-5692637df0f1

Cetaphil Daily Facial Moisturizer with suncreen SPF 50

UNIISPLATC D02BA

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

Identification

ManufacturerGalderma Laboratories, L.P.
CountryUS (United States)
ATC codeD02BA
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    0299493002
    1 TUBE in 1 CARTON (0299-4930-02) / 50 mL in 1 TUBE

Annotations

UNII (FDA Substance ID)
4Y5P7MUD51
OCTINOXATE
RxCUI 13369
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "4Y5P7MUD51",
    "rxcui": "13369",
    "inchikey": "YBGZDTIWKVFICR-JLHYYAGUSA-N",
    "display_name": "OCTINOXATE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "45d101be-2b88-4759-9ccc-556f5ec0553d": {
      "match": "brand_token",
      "title": "CETAPHIL REDNESS RELIEVING DAILY FACIAL MOISTURIZER WITH SUNSCREEN SPF 40 (TITANIUM DIOXIDE, ZINC OXIDE) CREAM [GALDERMA LABORATORIES, L.P.]",
      "spl_version": "4",
      "published_date": "2025-12-19"
    }
  },
  "productid": "0299-4930_0a1d0295-47d8-41f4-aaeb-5692637df0f1",
  "productndc": "0299-4930",
  "dosage_form": "LOTION",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "OCTINOXATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE; TITANIUM DIOXIDE",
  "proprietary_name": "Cetaphil Daily Facial Moisturizer with suncreen SPF 50",
  "active_ingred_unit": "mg/mL; mg/mL; mg/mL; mg/mL; mg/mL",
  "application_number": "M020",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "octinoxate, octisalate, octocrylene, oxybenzone, titanium dioxide",
  "start_marketing_date": "20120101",
  "active_numerator_strength": "75; 50; 70; 60; 57"
}

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