NDC 72934-4025

BETAMETHASONE DIPROPRIONATE 0.05% / MINOXIDIL 7%

Betamethasone Diproprionate 0.05% / Minoxidil 7%

BETAMETHASONE DIPROPRIONATE 0.05% / MINOXIDIL 7% is a Topical Solution in the Human Prescription Drug category. It is labeled and distributed by Sincerus Florida, Llc. The primary component is Betamethasone Dipropionate; Minoxidil.

• Product ID: 72934-4025_8875a838-5a95-3407-e053-2a95a90ae3eb
• NDC: 72934-4025
• Product Type: Human Prescription Drug
• Proprietary Name: BETAMETHASONE DIPROPRIONATE 0.05% / MINOXIDIL 7%
• Generic Name: Betamethasone Diproprionate 0.05% / Minoxidil 7%
• Dosage Form: Solution
• Route of Administration: TOPICAL
• Marketing Start Date: 2019-05-10
• Marketing Category: UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
• Labeler Name: Sincerus Florida, LLC
• Substance Name: BETAMETHASONE DIPROPIONATE; MINOXIDIL
• Active Ingredient Strength: 0 g/100g; g/100g
• Pharm Classes: Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 72934-4025-8

60 g in 1 BOTTLE, GLASS (72934-4025-8)

• Marketing Start Date: 2019-05-10
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 72934-4025-8 [72934402508]

BETAMETHASONE DIPROPRIONATE 0.05% / MINOXIDIL 7% SOLUTION

• Marketing Category: unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2019-05-10

Drug Details

Active Ingredients

Ingredient	Strength
BETAMETHASONE DIPROPIONATE	.05 g/100g

Pharmacological Class

• Corticosteroid [EPC]
• Corticosteroid Hormone Receptor Agonists [MoA]
• Arteriolar Vasodilation [PE]
• Arteriolar Vasodilator [EPC]
• Corticosteroid [EPC]
• Corticosteroid Hormone Receptor Agonists [MoA]
• Arteriolar Vasodilation [PE]
• Arteriolar Vasodilator [EPC]