Product Images Extra Strength Sunburn Relief
View Photos of Packaging, Labels & Appearance
Product Label Images
The following 8 images provide visual information about the product associated with Extra Strength Sunburn Relief NDC 69804-039 by Ridge Properties, such as packaging, labeling, and the appearance of the drug itself. This resource could be helpful for medical professionals, pharmacists, and patients seeking to verify medication information and ensure they have the correct product.
Dosage and Administration - Dosage and Administration
This text provides directions for using a topical pain reliever, advising the user to test the skin for sensitivity before applying it to the affected area as needed. It also warns the user to discontinue use if sensitivity occurs and notes that the product should not be used on the face.*
keep out of reach of children - OTC keep out of reach of children
This text is a warning label typically found on products that need to be kept away from children. It advises that the product is only intended for external use and must not come into contact with the eyes.*
Warnings - Warnings
This is a warning label for a product that should be kept out of reach of children. It is meant for external use only, and should not come into contact with the eyes.*
inactive ingredients - inactive ingredients section
This text lists the inactive ingredients present in a product. These include water, witch hazel, kava kava, organic yarrow, nutmeg, copaiba balsam, and BTMS 50, which is a natural extract.*
indications and usage - indications and usage
This text is too short to provide any context or details. It appears to be a fragment of a sentence related to pain relief. Based on this fragment, it can be inferred that it refers to a product or medication that is used for temporarily relieving pain. However, without more context, it is impossible to provide a useful description.*
package label - label
This is a description of a FDA registered topical anesthetic product. The product label warns the users not to use it if they have an allergy to any of its ingredients. It provides NDC# 69804-039-02 to identify it. The active ingredient is Lidocaine HCL 4%. It is not intended to be used on the face and should be discontinued if sensitivity occurs or if it lasts for over 7 days. The product is manufactured by Pain Organic and the company's contact information can be found at WWW.NATURALLYHL.COM. The product is made using Water, Witch Hazel, Organic Alcohol, Kava, Yarrow, Nutmeg, and Propolis as inactive ingredients.*
active ingredients - otc active ingredients section
This is a description of a product's active ingredients. The product contains Lidocaine HCL 4%. No further information regarding the product is available.*
purpose section - otc purpose section
This product is a topical anesthetic.*
* The product label images have been analyzed using a combination of traditional computing and machine learning techniques. It should be noted that the descriptions provided may not be entirely accurate as they are experimental in nature. Use the information in this page at your own discretion and risk.