Byd Antibacterial Wet Wipes (children)
Product Images NDC 75035-009

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 15 technical images submitted to the FDA as part of the official labeling for Byd Antibacterial Wet Wipes (children) (NDC 75035-009). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Byd Automative Industry Co., Ltd., 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

01_1 (01 1)

01_1 (01 1)
This text provides information about a product that is manufactured by BYD Auto Industry Company Limited and is distributed by Global Healthcare. It includes the contact details of the manufacturer's address in Pingshan, Shenzhen, China, and a telephone number. The website address of the manufacturer is also provided. The product is made in China. The last line of the text, "80 60004 ! 56032" is not clear and appears to be a code, which is not readable.*
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01_2 (01 2)

01_2 (01 2)
This text provides information about the manufacturer and distributor of a product. The product is manufactured by BYD Auto Industry Company Limited in Shenzhen, China and is distributed by Global Healthcare Product Solutions, LLC. The contact details for both the manufacturer and distributor are provided. No information is available about the specific product being described.*
FDA Label Image

02 (02)

02 (02)
This is a drug information label for a product containing Benzalkonium Chloride 0.13% (w/w), an antibacterial agent. The product is for external use only and is intended for handwashing to reduce bacteria on the skin. The label provides directions for use and cautionary warnings including keeping the product out of eyes, flushing thoroughly with water if it gets into the eyes, and seeking medical assistance if the product is ingested. The label also includes information on inactive ingredients and shelf life. The label model number is BZ-01.*
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03 (03)

03 (03)
This is a drug facts label for a product containing 0.13% Benzalkonium Chloride as an antibacterial agent for hand washing. It includes directions for use, warnings against eye contact, and instructions for discarding the product after the validity period. It also has a model number of BZ-01 and an expiration date of 2 years after the production date.*
FDA Label Image

04 (04)

04 (04)
This is a drug facts label describing the active ingredient, purpose, uses, directions, warnings, and other information about a product primarily designed for hand washing. The product contains Benzalkonium Chloride 0.13% and is intended for external use only. The label includes warnings regarding keeping product out of eyes and the reach of children, and instructions to seek medical help if swallowed. The product also contains several inactive ingredients and has an expiration date of 2 years after the date of production. Model number is BZ-01.*
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05 (05)

05 (05)
This is a drug information sheet with details about the active and inactive ingredients of a product containing Benzalkonium Chloride. The purpose of this antibacterial product is for hand washing to decrease bacteria on the skin. The user is cautioned to keep the product away from eyes and to seek medical help if swallowed. Children under 6 years must use the product under adult supervision. The product should be used within the validity period after opening. The expiration date is 2 years after the date of production. The model of the product is BZ-01.*
FDA Label Image

06 (06)

06 (06)
This is a Drug Facts label, with information on the active and inactive ingredients, purpose, warnings, directions, and expiration date of a product. The active ingredient is Benzalkonium Chloride, which has an antibacterial purpose. The product is intended for hand washing and reducing bacteria on the skin. The user is cautioned to keep the product out of the eyes, and to seek medical help if swallowed. The product should be used within the validity period, and is safe for children with adult supervision. There is a model number provided as BZ-01.*
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07 (07)

07 (07)
This is a Drug Facts label for BZ-01, a product containing 0.13% w/w of Benzalkonium Chloride, an antibacterial agent. It is recommended for hand washing to reduce bacteria on the skin. The user needs to wet their hands thoroughly with the product and allow it to dry. The label warns to keep the product away from the eyes, and to seek medical assistance immediately if it is swallowed. The product contains several inactive ingredients - Decyl glucoside, glycerin, methylparaben, propylparaben, phenoxyethanol, and water. The product should be used within its validity period, which is 2 years after the date of production.*
FDA Label Image

08 (08)

08 (08)
This is a drug fact sheet for a hand washing product containing Benzalkonium Chloride as an antibacterial agent. It is intended for external use only to decrease bacteria on the skin. The product must be kept away from eyes, and supervision is required when used on children under six years of age. In case of eye contact, washing thoroughly with water is advised. The product is also only meant for use within the specified validity period. The text also contains information on inactive ingredients, expiration date, and a model number.*
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09 (09)

09 (09)
This is a drug facts label for model BZ-01. It contains information about the active ingredient, benzalkonium chloride, its purpose which is to act as an antibacterial agent, its recommended use, which is to decrease bacteria on the skin through hand washing, and directions for use. The label also includes warnings for external use only, possible irritation or redness, instructions to keep the product out of eyes, and to seek medical help if the product has been swallowed, as well as information on inactive ingredients and product expiration date.*
FDA Label Image

10 (10)

10 (10)
This text is a Drug Facts label which provides information about the active and inactive ingredients used in a medication. The medication contains Benzalkonium Chloride as an active ingredient in a concentration of 0.13% (w/w), which acts as an antibacterial agent. The medicine is intended for hand washing purposes to reduce bacteria on the skin. The user must wet their hands with the product and let it dry. It is not intended for children under six years of age, and adult supervision is required. The product must be kept away from the eyes, and in case of contact with eyes, the user should flush their eyes with water. If there is any adverse reaction like irritation or redness, the use of the product should be stopped. The product must be used before its expiration date, which is two years after its production date. The text also includes the product model, which is BZ-01.*
FDA Label Image

11 (11)

11 (11)
This is a Drug Facts label for a product containing Benzalkonium Chloride as an active ingredient. It is intended for hand washing to reduce bacteria on the skin. The directions instruct one to wet hands thoroughly with the product and allow to dry. The label warns users to avoid contact with eyes and to seek medical help if swallowed. The product should be used within the validity period, and the expiration date is two years after the date of production. The label lists additional inactive ingredients. Model number BZ-01 is also provided.*
FDA Label Image

12 (12)

12 (12)
This is a drug fact sheet detailing an antibacterial hand wash containing 0.13% Benzalkonium Chloride. The product is intended for use on skin to reduce the presence of bacteria. The directions to use the product include wetting hands with the product and allowing them to dry; however, children under six must only use the product under adult supervision. The warning section notes that the product is for external use only, and should not come into contact with eyes. In case of eye contact, it should be flushed thoroughly with water, and medical help should be sought if the product is swallowed. The sheet lists the inactive ingredients, and the product validity period is recommended to be two years from the date of production. The model name of the product is BZ-01.*
FDA Label Image

13_1 (13 1)

13_1 (13 1)
This is a not-available description as the text seems to be a combination of gibberish and incomplete words. The text appears to be a mixed-up form of product labeling and does not provide any useful information.*
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13_2 (13 2)

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