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Bio-Scriptives Lidum Topical Analgesic Package Insert

Status:
Prescription (Rx) Facts
Strength:
2.8 g/56 g
Drug class:
Active ingredient:
Similar drugs:

Source: FDA drug labeling via NLM DailyMed · About this document

Prescribing information (package insert) - Bio-Scriptives Lidum Topical Analgesic

Drug Facts

Active Ingredients

Lidocaine 4%

Purpose

Local Analgesic

Uses

For the temporary relief of pain and itching due to:

  • minor burns
  • minor skin irritations
  • scrapes
  • minor cuts
  • sunburn
  • insect bites

Warnings

For external use only

When using this product

  • avoid contact with the eyes
  • do not use in large quantities, particularly over raw surfaces or blistered areas

Stop use and ask doctor if:

  • condition worsens
  • symptoms persist for more than 7 days
  • symptoms clear up and occur again within a few days

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Adults and children 2 years of age and older: Apply to the affected area not more than 3 to 4 times daily.
  • Children under 2 years of age: Consult a doctor.

Inactive Ingredients

Aloe, Water, Cholesterol, Isopropyl Myristate, Aqua Caprylic/Capric Triglyceride, Propylene Glycol, Hydrogenated Phosphatidylcholine, Glyceryl Stearate, PEG-100 Stearate, Arginine HCL, Ethyl Oleate, Propylene Glycol, Tocophersolan, Cetyl Alcohol, Triethanolamine, Xanthan Gum, Tocopherol, Allantoin, Aloe Barbadensis Leaf, Methylisothiazolinone, Methyl Nicotinate.

About this document

Source: FDA drug labeling via NLM DailyMed · Application number: OTC MONOGRAPH FINAL 346 · View the label on DailyMed

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Drug information for Bio-Scriptives Lidum Topical Analgesic

Rx or OTC
Prescription (Rx)?
  • This drug is available only with a prescription from a licensed healthcare provider.
  • Rx
Drug class Amide Local Anesthetic, Antiarrhythmic
Active ingredient Lidocaine 2.8 g/56 g
Dosage form Cream
Route Topical
Marketing status not in the current FDA NDC Directory
Company (applicant) Bio-Scriptives, Inc.
FDA approval OTC MONOGRAPH FINAL 346OTC monograph
Manufacturers 1 labelers list this drug on DailyMed
Packages (NDC)
Package
2.8 g/56 g – 56 g in 1 tube / 1 in 1 box NDC 60608-017-00
2.8 g/56 g – 4.5 g in 1 tube / 15 in 1 box NDC 60608-017-02

Source: FDA drug labeling via NLM DailyMed, data as of October 31, 2026. FDA data (DailyMed, Orange Book, Drug Shortages, enforcement reports). Not a substitute for the advice of a doctor or pharmacist.