Hand Sanitizer
Product Images NDC 78336-170

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Hand Sanitizer (NDC 78336-170). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Charles And Associates, Llc, 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

1 Liter Sample Label Sa

This is a bottle of Hand Sanitizer containing 1 liter (1000ml) or 33.8 fluid ounces.*

FDA Label Image

1 Fl Oz (30 mL) Ndc: 78336-070-01 (1oz(30ml)label 200630 Pf)

This is a hand sanitizer containing 70% ethyl alcohol, which is effective in reducing bacteria on the skin that can cause sickness. It is a moisturizing gel that kills 99% of germs. The product contains Carbopol 960, Triethanolamine, and Glycerin as inactive ingredients, and should be rubbed briskly onto both hands and allowed to dry. It should only be used externally and kept away from heat, flames, and contact with eyes, ears or mouth. If irritation develops, stop using it and contact a doctor. The product should be kept out of reach of children and should not be used on infants. It comes in a 1 fl oz (30 ml) bottle, with contact details provided in case of any queries.*

FDA Label Image

2.03 Fl Oz (60 mL) Ndc: 78336-070-02 (2.03oz(120ml)label 200612 Pf)

This is a drug fact label for a hand sanitizer product that contains 70% ethyl alcohol. It is intended for external use only as an antiseptic to reduce bacteria on the skin. The label warns that the product is flammable and should be kept away from heat and flame. If contact with the eyes, ears, or mouth occurs, the affected area should be flushed with water. The hand sanitizer should be applied to the palms and rubbed until dry. It is not suitable for infants, and children under 6 years old should be supervised when using it. The product is harmful to wood, and certain fabrics may become discolored. If irritation and redness persist for more than 72 hours, a doctor should be consulted. The label contains the manufacturer's contact information.*

FDA Label Image

16.9 Fl Oz (500 mL) Ndc: 78366-070-16 (Label 16.9oz 200609 Pf L)

This is a hand sanitizer that contains 70% ethyl alcohol which helps to reduce bacteria. It is for external use only and should not be used on infants. The hand sanitizer may discolor certain fabrics and is also harmful to wood finishes and plastics. Contact with eyes, ears, or mouth should be avoided. If contact does occur, flush with water. Keep out of reach of children, and if swallowed, one should get medical help or contact poison control immediately. It needs to be stored at room temperature and is made in Mexico.*

FDA Label Image

1 Gallon / 128 Fl Oz (3.79 Liters) Ndc: 78336-070-37 (Label 1gal 200609 Pf)

This is a Drug Facts label for a hand sanitizer that contains 70% Ethyl Alcohol as an active ingredient. The product is designed to help reduce bacteria on the skin that can cause sickness. It is flammable and should be kept away from heat and flame. The directions state to apply a small amount to the palms and rub briskly until dry, repeating as necessary. This product is not for infants and should be supervised for children under 6 years. If swallowed, the user should seek medical help immediately. The label also includes other information such as warnings, inactive ingredients, and contact information for questions or comments. The product is made in Mexico and is moisturizing gel with 1-gallon capacity.*

FDA Label Image

4.06 Fl Oz (120 mL) Ndc: 78336-070-04 (Label 4oz 200609 Pf L)

This is a drug facts label of a hand sanitizer manufactured in Mexico by an unknown entity. The active ingredient is ethyl alcohol, 70% v/v, which is an antiseptic, used to reduce the bacteria on the skin that can cause sickness; as such, it is recommended for repeated use. The product also contains demineralized water, carbopol 960, triethanolamine and glycerin as inactive ingredients. It should be kept at room temperature, it is flammable and should be kept away from heat and flame. On contact with certain fabrics, it may result in discoloration. It should be avoided from contact with eyes, ears, and mouth. In case of contact with these body parts, flush with water. The product should be kept out of reach of children; if swallowed, medical help should be contacted right away. The product is a moisturizing gel that comes in a 4.06 fl oz (120 ml) bottle. The label has a hotline number for questions and comments.*

FDA Label Image

8.45 Fl Oz (250 mL) Ndc: 78336-070-08 (Label 8.45oz 200609 Pf L)

This is a description of a hand sanitizer that contains Ethyl Alcohol, Carbopol 960, Triethanolamine and Glycerin. It is meant to help reduce bacteria on the skin that can cause sickness, and is recommended for repeated use. It should be stored at room temperature and kept away from heat and flame. Contact with eyes, ears, and mouth should be avoided, and it is not recommended to be used on infants. It is distributed by Charles & Associates, and made in Mexico. If irritation and redness persists, stop use and contact a doctor. It is important to keep it out of reach of children, and contact poison control if swallowed.*

* 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.