Lip Balm
Product Images NDC 62932-199

8 FDA label images from Private Label Select Ltd Co · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Lip Balm (NDC 62932-199). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Private Label Select Ltd Co, 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 Part 1 (Norwex Spf 15 Part I)

Label Part 1 (Norwex Spf 15 Part I)
Packaging label for Natural Sunscreen Lip Balm with Broad Spectrum SPF 15 by Private Label Select Ltd CO. The label states the product contains Zinc Oxide 10.5% as the active ingredient and is water resistant for 80 minutes. It includes caution warnings and directions for external use. The label lists manufacturing and distribution information for PLS in Taos, New Mexico, and Norwex USA Inc. in Coppell, TX.*
FDA Label Image

Label Part Ii (Norwex Spf 15 Part Ii)

Label Part Ii (Norwex Spf 15 Part Ii)
This Drug Facts panel continuation for LIP BALM includes directions for application before sun exposure and reapplication after swimming or sweating. It provides sun protection measures advising the use of Broad Spectrum sunscreens with SPF 15 or higher and limiting sun exposure during peak hours. The panel lists other ingredients such as sunflower seed oil, beeswax, coconut oil, shea butter, raspberry seed oil, cocoa seed butter, and additional oils. Contact information for questions or comments is also included.*
FDA Label Image

Active (Norwex Spf 15 Active)

Active (Norwex Spf 15 Active)
A Drug Facts panel excerpt showing the active ingredient Zinc Oxide 10.5% and its purpose as a sunscreen.*
FDA Label Image

Dosage (Norwex Spf 15 Dosage)

Dosage (Norwex Spf 15 Dosage)
Text panel continuing Drug Facts for LIP BALM. It includes directions to apply liberally 15 minutes before sun exposure, reapply after 80 minutes of swimming or sweating, and immediately after towel drying. The panel also covers sun protection measures, recommending broad spectrum sunscreens with SPF 15 or higher, limiting sun exposure time especially between 10 a.m. and 2 p.m., and wearing protective clothing such as long-sleeved shirts, pants, sunglasses, and broad-brimmed hats.*
FDA Label Image

Inactive (Norwex Spf 15 Inactive Ingredients)

Inactive (Norwex Spf 15 Inactive Ingredients)
This image shows a list of other ingredients for a product named LIP BALM by Private Label Select Ltd CO. Ingredients include sunflower seed oil, beeswax, caprylic/capric triglyceride, coconut oil, flavor, various plant butters and seed oils such as shea butter, raspberry seed oil, cacao seed butter, and tocopherol.*
FDA Label Image

Keep Out Of Reach (Norwex Spf 15 Keep Out Of Reach)

Keep Out Of Reach (Norwex Spf 15 Keep Out Of Reach)
This text panel provides safety warnings and instructions for the product LIP BALM by Private Label Select Ltd CO. It advises keeping the product out of reach of children, contacting poison control if swallowed, and consulting a healthcare professional before applying sunscreen to infants younger than 6 months.*
FDA Label Image

Purpose (Norwex Spf 15 Purpose)

Purpose (Norwex Spf 15 Purpose)
Drug Facts panel excerpt showing uses information, specifically noting that the product helps prevent sunburn.*
FDA Label Image

Warnings (Norwex Spf 15 Warnings)

Warnings (Norwex Spf 15 Warnings)
Warning panel text for LIP BALM by Private Label Select Ltd CO includes instructions for external use only, advises against use on damaged or broken skin, and cautions to keep out of eyes and out of reach of children. It instructs to rinse with water if it contacts eyes and to consult a doctor if rash occurs or poison control if ingested.*

* 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.