Jafra Daily
Product Images NDC 68828-053

2 FDA label images from Jafra Cosmetics International · 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 Jafra Daily (NDC 68828-053). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Jafra Cosmetics International, 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

Powder Fresh A-p 2oz Primary (Powder Fresh A P 2oz Primary)

Powder Fresh A-p 2oz Primary (Powder Fresh A P 2oz Primary)
Front and back label of JAFRA DAILY POWDER FRESH FOR WOMEN antiperspirant deodorant roll-on. The front label shows the product name, indication as antiperspirant deodorant roll-on, weight of 60 g (2 oz), and decorative purple swirl design. The back label includes usage warnings, active ingredient aluminum chlorohydrate, other ingredients in English and Spanish, manufacturer information Jafra Cosmetics International, and usage instructions.*
FDA Label Image

Powder Fresh A-p 2oz Secondary (Powder Fresh A P 2oz Secondary)

Powder Fresh A-p 2oz Secondary (Powder Fresh A P 2oz Secondary)
The packaging label for JAFRA DAILY POWDER FRESH FOR WOMEN Antiperspirant Deodorant Roll-on shows the product name and dosage form in English and Spanish. It specifies a net weight of 60 g (2 oz) and indicates the labeler as JAFRA COSMETICS INTERNATIONAL. The label also features usage instructions, active ingredient Aluminum Chlorohydrate 12.3%, warnings, and a list of inactive ingredients, with text in multiple languages including English, Spanish, German, and Italian.*

* 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.