Hydro 35

Product NDC

23710-035

11-digit product format

237100035

Labeler code

23710

Product ID

23710-035_a2ebc605-02a0-4ce1-b4c1-0d752094ad07

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Urea in a water and lipid based foam containing lactic acid

Dosage form

AEROSOL, FOAM

Route

TOPICAL

Labeler

Exeltis USA Dermatology, LLC

Marketing category

UNAPPROVED DRUG OTHER

Marketing start

2009-06-20

Marketing end

0000-00-00

Substance

UREA

Active strength

35 g/100g

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record