Active Ingredient
Benzalkonium Chloride 0.13%
The following Structured Product Label (SPL) was submitted to the FDA by Puretek Corporation for the product Diasinc (NDC 59088-596). 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 ingredient, purpose, uses, warnings, do not use on, 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.
Benzalkonium Chloride 0.13%
Antiseptic
■ a no-rinse topical antiseptic that protects against bacterial contamination
For external use only
■ deep or puncture wounds ■ animal bites ■ serious burns
■ do not get into eyes ■ If contact occurs, rinse eyes thoroughly with water.
■ If irritation or redness develops ■ condition persists for more than 72 hours
If swallowed, get medical help or contact a Poison Control Center right away.
■ spray soiled and/or odorous (body and/or perineal) areas ■ gently wipe clean ■ repeat as necessary until all soils are removed and skin is clean ■ pat dry (no rinsing necessary)
■ Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature]. ■ protect from freezing ■ avoid excessive heat
aloe barbadensis (aloe vera) leaf juice, aqua (purified water), butylene glycol, disodium EDTA, fragrance, GenRx Complex® [consisting of: bisabolol, calcium pantothenate (vitamin B5), Carthamus tinctorius (safflower) oleosomes, maltodextrin, niacinamide (vitamin B3), pyridoxine HCl (vitamin B6), silica, sodium ascorbyl phosphate (vitamin C), sodium starch octenylsuccinate, tocopheryl acetate (vitamin E), Zingiber officinale (ginger) root extract], glycerin, phenoxyethanol, polysorbate 20, sodium hyaluronate, sodium hydroxide.
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