Aruba Aloe Island Remedy Daily Ultra Aloe
Product Images NDC 53675-100

3 FDA label images from Aruba Aloe Balm Nv · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Aruba Aloe Island Remedy Daily Ultra Aloe (NDC 53675-100). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aruba Aloe Balm Nv, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Aruba Aloe 3 (Arubabox)

Aruba Aloe 3 (Arubabox)
Packaging label for ARUBA ALOE ISLAND REMEDY DAILY ULTRA ALOE CRÈME SPF 15. The label features branding elements including an aloe plant graphic and product information highlighting moisturizing properties and SPF 15 protection. It includes manufacturer details for Aruba Aloe Balm NV and a barcode on the lower panel.*
FDA Label Image

Aruba Aloe 2 (Arubadrugpanel)

Aruba Aloe 2 (Arubadrugpanel)
Drug Facts panel for ARUBA ALOE ISLAND REMEDY DAILY ULTRA ALOE showing active ingredients (Octinoxate 7.5%, Oxybenzone 4.5%) and their purpose as sunscreens. Includes uses, warnings for external use, directions for application, and a detailed list of inactive ingredients such as Aloe Vera Gel and botanical extracts.*
FDA Label Image

Aruba Aloe 1 (Arubajar)

Aruba Aloe 1 (Arubajar)
Label for ARUBA ALOE ISLAND REMEDY DAILY ULTRA ALOE CRÈME SPF 15, 4 oz (118 ml). The label includes directions to apply generously on skin before sun exposure and warnings for external use only, avoiding contact with eyes, and seeking medical help if swallowed. The product is from ARUBA ALOE BALM NV and highlights the use of fine aloe and an establishment date of 1890.*

* 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.