Chemical Structure (Sernivo 01)
Sernivo Spray
Product Images NDC 68040-714
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Sernivo (NDC 68040-714). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Primus Pharmaceuticals, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Figure A (Sernivo 02)
Figure B (Sernivo 03)
Figure C (Sernivo 04)
Figure D (Sernivo 05)
120 mL Carton Label (Sernivo 06)
This is a medication with the NDC code 6B040-714-28. It is a spray that contains 0.05% of betamethasone dipropionate. The potency of the medication is expressed as betamethasone. The medication is for topical use only and should not be used orally, ophthalmically, or intravaginally. The medication should be shaken well before use and applied to the skin twice daily. The medication should not be used for longer than two days. The medication is manufactured by PMS 299 PMS 261 Black and the expiration date can be found on the top of the carton or bottle label. The medication comes in a spray bottle and each gram contains 0.843 mg of betamethasone dipropionate.*
120 mL Spray Bottle Label (Sernivo 07)
Sernivo is a topical spray medication containing 0.05% betamethasone dipropionate which is for external use only to be applied twice daily on the affected skin after shaking well. The product should be discarded after 28 days of dispensation by the pharmacy. The medication should be kept out of children's reach and stored between 20°C to 25°C. Sernivo is manufactured by DPT Laboratories Ltd. and distributed by Primus Pharmaceuticals, Inc. Scottsdale AZ 85253.*
* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.
