Bio-scriptives Lidum
FDA Label NDC 60608-011

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Biochemics, Inc for the product Bio-scriptives Lidum (NDC 60608-011). 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, stop use if, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Lidocaine 5%



Purpose

Topical Anesthetic

Uses

■  rapid onset ■  temporary relief of pain and itching due to■  minor burns■  skin irritations■  scrapes■  cuts■  sunburn■  insect bites

Warnings

For external use only.

Do Not Use

■  in or near eyes■  in large quantities, particularly over raw surfaces or blistered areas

Stop Use If

■  allergic reaction occurs■  condition worses or does not improve within 7 days

Otc - Keep Out Of Reach Of Children

Keep out of the reach of children.

Directions

■  adults and children 2 years and up apply externally to affected areas 3-4 times a day.

Inactive Ingredients

Aloe Vera Juice, Water, Cholesterol, lsopropyl Myristate, Aqua and Caprylic Capric Triglyceride and Propylene Glycol and Hydrogenated Phosphatitylcholine, Glyceryl Stearate and PEG-100 Stearate, Arginine HCI, Ethyl OLeate, Propylene Glycol, dAlpha-Tocopheryl Polyethylene Glycol-1000 Succinate, Cetyl Alcohol,  Triethanolamine, Xanthan Gum, Vitamin E, Allantoin, Aloe Vera Powder, Methylisothiazolinone, Methyl Nicotinate

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