Aquaphor Itch Relief

UNIISPLATC A07EA02

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

Identification

ManufacturerBeiersdorf Inc

CountryUS (United States)

ATC codeA07EA02

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 6

ndc11
1035612004
28 g in 1 TUBE (10356-120-04)
ndc11
1035612007
56 g in 1 TUBE (10356-120-07)
ndc11
1035612030
.9 g in 1 PACKET (10356-120-30)
ndc11
1035612052
1 TUBE in 1 CARTON (10356-120-52) / 28 g in 1 TUBE (10356-120-04)
ndc11
1035612053
2 TUBE in 1 CARTON (10356-120-53) / 28 g in 1 TUBE (10356-120-04)
ndc11
1035612054
1 TUBE in 1 CARTON (10356-120-54) / 56 g in 1 TUBE (10356-120-07)

Annotations

UNII (FDA Substance ID)

WI4X0X7BPJ

HYDROCORTISONE

RxCUI 5492

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "WI4X0X7BPJ",
    "rxcui": "5492",
    "inchikey": "JYGXADMDTFJGBT-VWUMJDOOSA-N",
    "display_name": "HYDROCORTISONE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "TOPICAL",
  "spl_meta": {
    "b1d0333f-ba60-35d8-e053-2995a90af932": {
      "match": "brand_token",
      "title": "AQUAPHOR ITCH RELIEF (HYDROCORTISONE) OINTMENT [BEIERSDORF INC]",
      "spl_version": "6",
      "published_date": "2025-12-18"
    }
  },
  "productid": "10356-120_4615f353-0a2d-5ff1-e063-6394a90a77e3",
  "productndc": "10356-120",
  "dosage_form": "OINTMENT",
  "dea_schedule": null,
  "product_type": "HUMAN OTC DRUG",
  "substance_name": "HYDROCORTISONE",
  "proprietary_name": "Aquaphor Itch Relief",
  "active_ingred_unit": "g/100g",
  "application_number": "M017",
  "marketing_category": "OTC MONOGRAPH DRUG",
  "nonproprietary_name": "Hydrocortisone",
  "start_marketing_date": "20201101",
  "active_numerator_strength": "1"
}

Related drugs

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