NDC 72934-1088

ASCORBYL PALMITATE 2% / HYALURONIC ACID SODIUM SALT 0.2% / NIACINAMIDE 5% / TRETINOIN 0.025%

Ascorbyl Palmitate 2% / Hyaluronic Acid Sodium Salt 0.2% / Niacinamide 5% / Tretinoin 0.025%

ASCORBYL PALMITATE 2% / HYALURONIC ACID SODIUM SALT 0.2% / NIACINAMIDE 5% / TRETINOIN 0.025% is a Topical Gel in the Human Prescription Drug category. It is labeled and distributed by Sincerus Florida, Llc. The primary component is Niacinamide; Tretinoin; Hyaluronate Sodium.

Product ID72934-1088_891a69a7-e046-c8c5-e053-2995a90ab49e
NDC72934-1088
Product TypeHuman Prescription Drug
Proprietary NameASCORBYL PALMITATE 2% / HYALURONIC ACID SODIUM SALT 0.2% / NIACINAMIDE 5% / TRETINOIN 0.025%
Generic NameAscorbyl Palmitate 2% / Hyaluronic Acid Sodium Salt 0.2% / Niacinamide 5% / Tretinoin 0.025%
Dosage FormGel
Route of AdministrationTOPICAL
Marketing Start Date2019-05-17
Marketing CategoryUNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
Labeler NameSincerus Florida, LLC
Substance NameNIACINAMIDE; TRETINOIN; HYALURONATE SODIUM
Active Ingredient Strength5 g/100g; g/100g; g/100g
Pharm ClassesRetinoid [EPC],Retinoids [CS]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 72934-1088-2

30 g in 1 BOTTLE, PUMP (72934-1088-2)
Marketing Start Date2019-05-17
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 72934-1088-2 [72934108802]

ASCORBYL PALMITATE 2% / HYALURONIC ACID SODIUM SALT 0.2% / NIACINAMIDE 5% / TRETINOIN 0.025% GEL
Marketing Categoryunapproved drug other
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-05-17

Drug Details

Active Ingredients

IngredientStrength
NIACINAMIDE5 g/100g

OpenFDA Data

SPL SET ID:891a69a7-e045-c8c5-e053-2995a90ab49e
Manufacturer
UNII

Pharmacological Class

  • Retinoid [EPC]
  • Retinoids [CS]
  • Retinoid [EPC]
  • Retinoids [CS]

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