Active Ingredients
Benalkonium chloride (0.13%)
Antiseptic Wipes
FDA Label NDC 72308-015
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Flex Beauty Labs for the product Antiseptic Wipes (NDC 72308-015). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredients, purpose, use, warnings, do not use, when using this product, stop use and ask a doctor if, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antibacterial
Use
Use to reduce bacteria on the skin
Warnings
For external use only
Do Not Use
Do not use if you are allegic to any of the ingredients.
When Using This Product
When using this product do not use in or near eyes.
In cases of contact, rinse eyes thoroughly with water.
Stop Use And Ask A Doctor If
Stop use and ask a doctor if irritation or redness develops.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contqact a Poison Control Center right away
Directions:
- Adults and children over 2 yeas of age:Apply to hands. Allow to dry without wioing.
- Children under 2 year of age:ask doctor prior to use
Inactive Ingredients
water, glycerin, sodium PCA, Aloe barbadensis leaf juice, fragrance, polysorbate 20, tetrasodium EDTA, phenoxyethanol, ethylhexylglycerin, citric acid
Principal Display Panel
60 WIPES
14 X 19 cm
5.5 IN X 7.4 IN
Wips2 (Wips2)
20 WIPES
14 X 19 cm
5.5 IN X 7.4 IN
Wips1 (Wips1)
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