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Drug Facts
The following Structured Product Label (SPL) was submitted to the FDA by Natureplex Llc for the product Proplex Lidocaine (NDC 67234-052). 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 other, active ingredient, purpose, use, warnings, otc - do not use, stop use and ask a doctor if, otc - pregnancy or breast feeding, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Drug Facts
Lidocaine 4%
Topical analgesic
for the temporary relief of pain associated with minor burns, sunburn, minor cuts, scrapes, insect bites, and minor skin irritations
For external use only.
Avoid contact with eyes.
Not for prolonged use.
Do not use in large quantities, particularly over raw surfaces or blistered areas.
If pregnant or breast-feeding, ask a health professional before use.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away: 800-222-1222.
Adults and children 2 years of age and older:
Children under 2 years of age:
Aloe barbadensis leaf juice, arginine, benzophenone-4, caprylyl glycol, cetyl alcohol, dimethyl sulfoxide, hexylene glycol, melaleuca alternifolia (tea tree) leaf oil, phenoxyethanol, potassium sorbate, purified water, simmondsia chinensis (jojoba) seed oil, sodium polyacrylate, stearic acid
866-323-0107 or www.natureplex.com
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