NDC 72934-6225

141016 HYDROCORTISONE 0.5% / HYDROQUINONE 4% / TRETINOIN 0.025%

141016 Hydrocortisone 0.5% / Hydroquinone 4% / Tretinoin 0.025%

141016 HYDROCORTISONE 0.5% / HYDROQUINONE 4% / TRETINOIN 0.025% is a Topical Emulsion in the Human Prescription Drug category. It is labeled and distributed by Sincerus Florida, Llc. The primary component is Hydroquinone; Hydrocortisone; Tretinoin.

Product ID72934-6225_a97c74e8-0133-1209-e053-2995a90a8592
NDC72934-6225
Product TypeHuman Prescription Drug
Proprietary Name141016 HYDROCORTISONE 0.5% / HYDROQUINONE 4% / TRETINOIN 0.025%
Generic Name141016 Hydrocortisone 0.5% / Hydroquinone 4% / Tretinoin 0.025%
Dosage FormEmulsion
Route of AdministrationTOPICAL
Marketing Start Date2020-07-02
Marketing CategoryUNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
Labeler NameSincerus Florida, LLC
Substance NameHYDROQUINONE; HYDROCORTISONE; TRETINOIN
Active Ingredient Strength4 g/100g; g/100g; g/100g
Pharm ClassesMelanin Synthesis Inhibitor [EPC],Melanin Synthesis Inhibitors [MoA],Depigmenting Activity [PE],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Retinoid [EPC],Retinoids [CS]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 72934-6225-2

30 g in 1 BOTTLE, PUMP (72934-6225-2)
Marketing Start Date2020-07-02
NDC Exclude FlagN
Sample Package?N

Drug Details


© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.