The Man By Vanibiss Razor Bumps Serum
Product Images NDC 81890-005

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for The Man By Vanibiss Razor Bumps Serum (NDC 81890-005). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Vanibiss 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.

FDA Label Image

Razor Bumps Box (Fd 04418 The Man By Vanibiss Razor Bumps Serum Roll On Box 81890 005 03)

Razor Bumps Box (Fd 04418 The Man By Vanibiss Razor Bumps Serum Roll On Box 81890 005 03)
THE MAN BY VANIBISS RAZOR BUMPS SERUM packaging label shows a roll-on serum for men, 3.5 fl. oz / 103 mL. The label highlights it is a targeted solution to reduce post-shave irritation and hydrate skin. Active ingredient is allantoin 0.5% as a skin protectant. Labeler is Vanibiss Inc, made in the USA, with drug facts and usage instructions included.*
FDA Label Image

Razor Bumps Roll On (Fd 04418 The Man By Vanibiss Razor Bumps Serum Roll On Tube 81890 005 03)

Razor Bumps Roll On (Fd 04418 The Man By Vanibiss Razor Bumps Serum Roll On Tube 81890 005 03)
Drug Facts panel for THE MAN BY VANIBISS RAZOR BUMPS SERUM includes active ingredient Allantoin 0.5% as a skin protectant. It temporarily protects and relieves chapped or cracked skin. Warnings cover external use only, avoiding use in children under 12 without doctor direction, and avoiding eyes. Instructions include stopping use and consulting a doctor if conditions worsen or symptoms persist. Not for use on deep wounds, animal bites, or serious burns. Additional details provide inactive ingredients, manufacturing info, directions, and contact information.*

* 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.