NDC 72934-4023

BETAMETHASONE DIPROPIONATE 0.05% / MINOXIDIL 5%

Betamethasone Dipropionate 0.05% / Minoxidil 5%

BETAMETHASONE DIPROPIONATE 0.05% / MINOXIDIL 5% is a Topical Solution in the Human Prescription Drug category. It is labeled and distributed by Sincerus Florida, Llc. The primary component is Minoxidil; Betamethasone Dipropionate.

• Product ID: 72934-4023_8747c1ea-6b25-46c8-e053-2995a90a33df
• NDC: 72934-4023
• Product Type: Human Prescription Drug
• Proprietary Name: BETAMETHASONE DIPROPIONATE 0.05% / MINOXIDIL 5%
• Generic Name: Betamethasone Dipropionate 0.05% / Minoxidil 5%
• Dosage Form: Solution
• Route of Administration: TOPICAL
• Marketing Start Date: 2019-05-01
• Marketing Category: UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
• Labeler Name: Sincerus Florida, LLC
• Substance Name: MINOXIDIL; BETAMETHASONE DIPROPIONATE
• Active Ingredient Strength: 5 g/100g; g/100g
• Pharm Classes: Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 72934-4023-8

60 g in 1 BOTTLE, GLASS (72934-4023-8)

• Marketing Start Date: 2019-05-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 72934-4023-8 [72934402308]

BETAMETHASONE DIPROPIONATE 0.05% / MINOXIDIL 5% SOLUTION

• Marketing Category: unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: GM
• Marketing Start Date: 2019-05-01

Drug Details

Active Ingredients

Ingredient	Strength
MINOXIDIL	5 g/100g

Pharmacological Class

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