![DICLOFENAC SODIUM 3% / HYALURONIC ACID SODIUM SALT 2% / NIACINAMIDE 4% GEL [SINCERUS FLORIDA, LLC]](https://medic.hrt.org//dailymed/images/883dde9f-e5dd-69d9-e053-2a95a90a2c24/-2 end.jpg)
![DICLOFENAC SODIUM 3% / HYALURONIC ACID SODIUM SALT 2% / NIACINAMIDE 4% GEL [SINCERUS FLORIDA, LLC]](https://medic.hrt.org//dailymed/images/883dde9f-e5dd-69d9-e053-2a95a90a2c24/1072-2 front.jpg)
![DICLOFENAC SODIUM 3% / HYALURONIC ACID SODIUM SALT 2% / NIACINAMIDE 4% GEL [SINCERUS FLORIDA, LLC]](https://medic.hrt.org//dailymed/images/883dde9f-e5dd-69d9-e053-2a95a90a2c24/1072-2 middle.jpg)
| NDC | 72934-1072-2 |
| Set ID | 883dde9f-e5dd-69d9-e053-2a95a90a2c24 |
| Category | HUMAN PRESCRIPTION DRUG LABEL |
| Packager | Sincerus Florida, LLC |
| Generic Name | |
| Product Class | |
| Product Number | |
| Application Number |
- Directions for use
- Sincerus Florida. Adverse reactions
- Active, inactive
- NDC 72934-1072-2 DICLOFENAC SODIUM 3% / HYALURONIC ACID SODIUM SALT 2% / NIACINAMIDE 4% Gel 30 gm
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INGREDIENTS AND APPEARANCE
DICLOFENAC SODIUM 3% / HYALURONIC ACID SODIUM SALT 2% / NIACINAMIDE 4%
diclofenac sodium 3% / hyaluronic acid sodium salt 2% / niacinamide 4% gelProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:72934-1072 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DICLOFENAC SODIUM (UNII: QTG126297Q) (DICLOFENAC - UNII:144O8QL0L1) DICLOFENAC SODIUM 3 g in 100 g Product Characteristics Color white (clear gel) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72934-1072-2 30 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/07/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/07/2019 Labeler - Sincerus Florida, LLC (080105003) Establishment Name Address ID/FEI Business Operations Sincerus Florida, LLC 080105003 manufacture(72934-1072)
