NDC 72934-6121

HYDROQUINONE 8%

Hydroquinone 8%

HYDROQUINONE 8% is a Topical Emulsion in the Human Prescription Drug category. It is labeled and distributed by Sincerus Florida, Llc. The primary component is Hydroquinone.

• Product ID: 72934-6121_874c1900-82ed-4082-e053-2995a90aff22
• NDC: 72934-6121
• Product Type: Human Prescription Drug
• Proprietary Name: HYDROQUINONE 8%
• Generic Name: Hydroquinone 8%
• Dosage Form: Emulsion
• 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: HYDROQUINONE
• Active Ingredient Strength: 8 g/100g
• Pharm Classes: Melanin Synthesis Inhibitor [EPC],Melanin Synthesis Inhibitors [MoA],Depigmenting Activity [PE]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 72934-6121-2

30 g in 1 BOTTLE, PUMP (72934-6121-2)

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

NDC SPL Data Element Entries

NDC 72934-6121-2 [72934612102]

HYDROQUINONE 8% EMULSION

• 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
HYDROQUINONE	8 g/100g

Pharmacological Class

• Melanin Synthesis Inhibitor [EPC]
• Melanin Synthesis Inhibitors [MoA]
• Depigmenting Activity [PE]
• Melanin Synthesis Inhibitor [EPC]
• Melanin Synthesis Inhibitors [MoA]
• Depigmenting Activity [PE]