Hand Sanitizer
Product Images NDC 49852-602

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 49852-602). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Tri-coastal Design Company 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.

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FDA Label Image

Package Label (Hndsntzr62lghtpnk)

Package Label (Hndsntzr62lghtpnk)
This is a drug label for a hand sanitizer product called "Batoh#20200109", which is distributed and manufactured by WMMI NJO7e N\ Msrmed. The sanitizer has a 62% alcohol denat concentration to decrease bacteria on the skin. It is recommended for repeated use and comes in contact with eyes and mucous membranes. In case of contact, rinse area thoroughly with water. Keep away from children, flames or fire. The sanitizer should be used externally and does not contain grain alcohol. If ingested, one should contact a doctor or Poison Control Center immediately. The product should be applied in a dime sized amount and rubbed between hands until dry. The inactive ingredients of Batoh#20200109 are water, fragrance, PEG40 Hydrogenated Castor Oil, Acrylates C10-30 Alkyl Acrylate Crosspolymer, Sodium Hydroxide, Denatonium Benzoate, DBC Red No33 (CI 17200). It should be stored below 105°F. For further queries, one may contact 01-800-278-9218.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.