Cetaphil Soothing Gel Cream

UNIISPL

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

Identification

ManufacturerGalderma Laboratories, L.P.

CountryUS (United States)

ATC code—

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 4

ndc11
0299410500
10 g in 1 TUBE (0299-4105-00)
ndc11
0299410505
85 g in 1 TUBE (0299-4105-05)
ndc11
0299410510
226 g in 1 TUBE (0299-4105-10)
ndc11
0299410515
453 g in 1 JAR (0299-4105-15)

Annotations

UNII (FDA Substance ID)

344S277G0Z

ALLANTOIN

RxCUI 508

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "344S277G0Z",
    "rxcui": "508",
    "inchikey": "POJWUDADGALRAB-UHFFFAOYSA-N",
    "display_name": "ALLANTOIN",
    "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": "0299-4105_123cee2b-1cfd-4530-bce4-bd524177fcdd",
  "productndc": "0299-4105",
  "dosage_form": "CREAM",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "ALLANTOIN",
  "proprietary_name": "Cetaphil Soothing Gel Cream",
  "active_ingred_unit": "mg/g",
  "application_number": "M016",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "allantoin",
  "start_marketing_date": "20200217",
  "active_numerator_strength": "5"
}

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