Stellalife Vega Oral Care Spray
Product Images NDC 69685-121

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Stellalife Vega Oral Care (NDC 69685-121). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Stellalife, 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

Label 1 (01 Spray Unflavored Label)

Label for StellaLife VEGA Oral Care Spray, an oral spray for pain and swelling relief, promoting healing and reducing bruising. The label shows it is unflavored and contains 1 fluid ounce (30 ml). The active ingredients listed include Arnica 3X, Calendula 3X, Chamomilla 5X, Echinacea angustifolia 3X, Echinacea purpurea 3X, Hepar sulph calc 8X, Hypericum 10X, Ignatia 30X, Ledum palustre 6X, Ruta 12X, Silicea 8X, and Staphysagria 8X. The labeler is StellaLife, Inc.*

FDA Label Image

Label 2 (02 Spray Unflavored Label)

This image shows a continuation of the Drug Facts panel for StellaLife VEGA Oral Care Pain and Swelling Relief spray. It includes sections on Uses, Warnings, and Directions, detailing its temporary relief of pain, swelling, and bruising, allergy warnings, and instructions for oral spray use under the tongue for adults and children over 6 years.*

FDA Label Image

Label 3 (03 Spray Unflavored Label)

Drug facts panel for StellaLife VEGA Oral Care Pain and Swelling Relief spray, including other information about tamper-evident seals, storage instructions, and product use timeline. Lists inactive ingredients such as citric acid, glycerin, and potassium sorbate. Provides contact information for questions and a disclaimer about claims based on traditional homeopathic practice not evaluated by the FDA.*

* 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.