Neutrogel
Product Images NDC 77251-008

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Neutrogel (NDC 77251-008). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Quimica Rosmar S.a De C.v, 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

1000 mL (Neutrogel Fda (1000 mL) Master Label 021220)

1000 mL (Neutrogel Fda  (1000 mL) Master Label 021220)
This is a label for a product called NEUTROGEL which contains Benzethonium chloride 0.10%(w/w) as an antiseptic agent. It is intended for washing and sanitizing hands to help reduce bacteria on the skin that may cause disease. There are warnings included such as not using the product on children less than 2 months old or on open skin wounds. If irritation or redness persists, the use of the product should be stopped and a doctor should be contacted. The label includes directions for use and a list of inactive ingredients. There is contact information for the manufacturer provided.*
FDA Label Image

20000 mL (Neutrogel Fda (20 L) Master Label 021220)

20000 mL (Neutrogel Fda  (20 L) Master Label 021220)
This is a drug facts label that provides information about an antiseptic product containing Benzethonium chloride 0.10%. The product is meant for washing and sanitizing hands and helps reduce bacteria on the skin that can cause disease. The label provides warnings regarding not using the product on children under two months of age, open skin wounds, and to contact a doctor if irritation or redness persists. The label also provides directions for use and lists inactive ingredients. The product is residue-free and comes in a 20L container. Contact information for the manufacturer is provided for any questions or comments.*
FDA Label Image

200000 mL (Neutrogel Fda (200l) Master Label 021220)

200000 mL (Neutrogel Fda  (200l) Master Label 021220)
This is a label of a product that contains benzethonium chloride as an active ingredient with a concentration of 0.10% (w/w). It is intended to be used as an antiseptic for washing and sanitizing hands to help reduce bacteria on the skin that can potentially cause disease. The product should not be used on open skin wounds, on children younger than 2 months of age, or if irritation or redness persists for more than 72 hours. The directions mention wetting the hands, placing enough product in the hand, rubbing gently for at least 30 seconds, washing skin, rinse thoroughly and dry. The label also has information about the product such as its weight, inactive ingredients, and company contact information.*
FDA Label Image

250 mL (Neutrogel Fda (250 mL) Master Label 021220 Ab)

FDA Label Image

(4000 mL) (Neutrogel Fda (4 L) Master Label 021220)

(4000 mL) (Neutrogel Fda  (4 L) Master Label 021220)
This is a label of a product called "NEUTROGEL 4L" manufactured by Quimica Rosmar. It contains Benzethonium chloride 0.10% (w/w) as the active antiseptic ingredient that helps reduce bacteria on skin. It is used for washing and sanitizing hands. This should not be used on children less than 2 months of age and on open skin wounds. In case of any irritation or redness, consult a doctor. It is meant for external use only and should not be swallowed. The product contains water, sodium lauryl ether sulfate, and other inactive ingredients. For further details, visit www.rosmar-usa.com, or contact 1-833-4-ROSMAR for any queries or comments.*
FDA Label Image

500 mL (Neutrogel Fda (500 mL) Master Label 021220)

500 mL (Neutrogel Fda  (500 mL) Master Label 021220)
This is a label for a hand sanitizer product with benzethonium chloride 0.10% as the active ingredient. It is intended for washing and sanitizing hands and reducing bacteria that may cause disease. The label warns to avoid using the product on children under two months of age and open skin wounds. If irritation or redness persists, stop use and contact a doctor. The label provides directions for use and lists the inactive ingredients, and includes the manufacturer's contact information.*

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