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FDA Approval

VANOXIDE

FDA-approved pharmaceutical product with comprehensive regulatory information, manufacturing details, and complete labeling documentation.

FDA Approval Summary

Company
Effective Date
October 9, 2023
Labeling Type
HUMAN PRESCRIPTION DRUG LABEL
Benzoyl peroxide(5 g in 100 g)
Hydrocortisone(0.5 g in 100 g)

Products1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

VANOXIDE HC

Product Details

NDC Product Code
11086-032
Route of Administration
TOPICAL
Effective Date
October 9, 2023
Code: W9WZN9A0GMClass: ACTIBQuantity: 5 g in 100 g
Code: WI4X0X7BPJClass: ACTIBQuantity: 0.5 g in 100 g
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