Treatonic Tattoo Numbing Cream
Product Images NDC 71331-118
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Product Visual Gallery
This gallery contains 12 technical images submitted to the FDA as part of the official labeling for Treatonic Tattoo Numbing Cream (NDC 71331-118). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Orange Lab, 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.
Product Images & Figures Index
Stopifdoc (Stop Using And Ask A Doc)
This text instructs the reader to stop using the product and consult a doctor if discomfort persists for 7 days or if symptoms such as redness, irritation, swelling, pain, or other symptoms develop or worsen. It emphasizes the importance of seeking medical advice if the symptoms being treated do not improve.*
Uses Purpose (Uses)
Contactus (Contact Us)
This text provides contact information for customer care services. Customers can reach out for solutions by emailing [email protected].*
Directions (Directions)
This text provides directions for using a particular product for adults. It advises cleansing the affected area with mild soap and warm water, then drying with toilet tissue or a soft cloth before applying the product up to 4 times a day. For children under 12, it recommends consulting a doctor before use.*
Warning_donotuseif (Do Not Use If Pregnant Warnings)
This text is a warning label for a product that states it is for external use only. It advises pregnant or breastfeeding individuals to consult a health professional before using the product. It also warns against allergic reactions and accidental overdose, recommending seeking medical help or contacting poison control in case of an overdose.*
Inactiveing (Inactive Ing)
This is a list of inactive ingredients in a product. The ingredients include DI Water, Dimethyl Isosorbide, Ethylhexyl Palmitate, Hydrogenated Polydecene, Propylene Glycol, Arnica Montana Flower Extract, Sunflower Seed Oil, Emu Oil, Phenoxyethanol, Menthol, Allantoin, Vitamin E (Tocopheryl Acetate), and more. These ingredients are commonly found in skincare or topical products.*
Keepoutofreach (Keep Out Of Reach Of Children)
Label01 (Label01)
This is a description of a topical analgesic product containing lidocaine as the active ingredient. It is used for the temporary relief of pain and itching associated with minor skin irritations, burns, cuts, scrapes, and insect bites. The product is to be used externally only. It provides long-lasting and maximum strength numbing relief. Directions for use include cleansing the affected area before applying the product up to 4 times a day for adults, with consultation required for children under 12. The product warns against allergic reactions, overdose, and discomfort lasting more than 7 days. Inactive ingredients include water, various extracts, and emollients. Additionally, it advises storing the product at a temperature range of 59°F-86°F and not in direct sunlight. It also recommends seeking medical attention if accidentally ingested and provides customer care contact information.*
Label02 Box (Label02 Box)
Otherinfo (Other Information)
Whenusing (When Using This Product)
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.