NDC 23710-035

Hydro 35

Urea In A Water And Lipid Based Foam Containing Lactic Acid

Hydro 35 is a Topical Aerosol, Foam in the Human Prescription Drug category. It is labeled and distributed by Exeltis Usa Dermatology, Llc. The primary component is Urea.

• Product ID: 23710-035_a2ebc605-02a0-4ce1-b4c1-0d752094ad07
• NDC: 23710-035
• Product Type: Human Prescription Drug
• Proprietary Name: Hydro 35
• Generic Name: Urea In A Water And Lipid Based Foam Containing Lactic Acid
• Dosage Form: Aerosol, Foam
• Route of Administration: TOPICAL
• Marketing Start Date: 2009-06-20
• Marketing Category: UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
• Labeler Name: Exeltis USA Dermatology, LLC
• Substance Name: UREA
• Active Ingredient Strength: 35 g/100g
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 23710-035-15

1 CANISTER in 1 CARTON (23710-035-15) > 150 g in 1 CANISTER

• Marketing Start Date: 2009-06-20
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 23710-035-15 [23710003515]

Hydro 35 AEROSOL, FOAM

• Marketing Category: Unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: GM
• Marketing Start Date: 2009-06-20
• Marketing End Date: 2020-01-20

NDC 23710-035-20 [23710003520]

Hydro 35 AEROSOL, FOAM

• Marketing Category: Unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2009-06-20
• Marketing End Date: 2020-01-20

Drug Details

Active Ingredients

Ingredient	Strength
UREA	35 g/100g

OpenFDA Data

• SPL SET ID: c1fc0ed7-6383-455a-98c3-ef44b312fc0d
• Manufacturer:
  • Exeltis USA Dermatology, LLC
• UNII:
  • 8W8T17847W
• RxNorm Concept Unique ID - RxCUI:
  • 849650
  • 849646