Medicine guide

Caring Mill Lidocaine Aloe Gel Burn and Pain Relief

5 mg/mL · Liquid

  • Available without prescription
  • Amide Local Anesthetic
Active substance
Lidocaine Hydrochloride
Made by
FSA Store Inc.

Quoted from the official source. Not yet reviewed by Mediclarum — the leaflet in your pack is authoritative.

At a glance

Quoted from the official label · 2024-01-12

The FDA lists a current shortage of lidocaine hydrochloride

Not necessarily this product — shortages are reported per presentation. Your pharmacy will know. · Updated 2026-09-22 FDA drug shortages

What it is

External Analgesic

Used for
  • For the temporary relief of pain and itching associated with minor burns, sunburn, minor cuts, scrapes, insect bites, or minor skin irritations.
Do not take it if

In large quantities, particularly over raw surfaces or blistered areas.

All warnings ↓
Good to know
  • Sold without a prescription
  • FDA enforcement reports list no ongoing recall, and none from the last two years, for this product code · checked 2026-10-02
274other products contain Lidocaine Hydrochloride — compare makers, forms and strengths

Every line above is selected, not written, from the official label. Nothing is reworded. DailyMed

What it is for

  • For the temporary relief of pain and itching associated with minor burns, sunburn, minor cuts, scrapes, insect bites, or minor skin irritations.

From the official label · 2024-01-12 · DailyMed

How it works

From the US prescribing label for the same active substance (LIDOCAINE). It describes the substance, not this exact product.

Lidocaine stabilizes the neuronal membrane by inhibiting the ionic fluxes required for the initiation and conduction of impulses, thereby effecting local anesthetic action.

Half-life1.5–2.0 h
Mostly cleared after≈ 8.8 hfive half-lives — our arithmetic
How the body breaks it down

Lidocaine is metabolized rapidly by the liver, and metabolites and unchanged drug are excreted by the kidneys.

Quoted from the prescribing label, sections “Mechanism of Action” and “Pharmacokinetics”. DailyMed · 2026-08-31

Do not take it if

in large quantities, particularly over raw surfaces or blistered areas.

Quoted from the official label, section “OTC — Do Not Use”.

How to take it

These directions are for this exact strength and form. Another one is different.

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

Quoted from the official label, section “Dosage & Administration”.

Other warnings

  • For external use only
  • Avoid contact with eyes If condition worsens , or
  • if symptoms persist for more than 7 days or clear up and occur again with a few days, discontinue use of this product and consult a doctor.
  • Do not use in large quantities, particularly over raw surfaces or blistered areas.
  • Keep out of reach of children.

Quoted from the official label, section “Warnings”.

Keep away from children

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

Quoted from the official label, section “OTC — Keep Out of Reach of Children”.

What kind of medicine it is

External Analgesic

Quoted from the official label, section “OTC — Purpose”.

Other ingredients

Relevant if you react to a dye, a preservative, lactose or gluten.

Water, Aloe Barbadensis Leaf Extract, Glycerin, Sodium Hydroxide, Propylene Glycol, Glyceryl Acrylate/Acrylic Acid Copolymer, Carbomer, Phenoxyethanol, Polysorbate 20, Caprylyl Glycol, Allantoin, Panthenol, Citrus Limon (Lemon) Peel Extract, Mentha Viridis (Spearmint) Leaf Oil, Symphytum Officinale (Comfrey) Leaf Extract, Tocopheryl Acetate, 1,2-Hexanediol, Ethylhexylglycerin, Blue 1, Yellow 5.

Quoted from the official label, section “Inactive Ingredients”.

Ingredients people check for

Lactose, gluten, dyes, sugars and other ingredients that matter with an allergy, intolerance or diet — as this product’s FDA label lists them.

This label’s list of inactive ingredients names none of: lactose, wheat or gluten, colour dyes, sugars, sugar alcohols, alcohol (ethanol), aspartame (phenylalanine), gelatin, peanut oil, soy, parabens, sulfites, titanium dioxide.

Quoted from the FDA label. A label that does not name an ingredient is not a guarantee that the product is free of it, and formulations change. With an allergy, check the pack and ask a pharmacist.

Same active substance, strength and form in other countries

Matched on active substance, strength and kind of form only. This is not a statement that the products are equivalent or interchangeable: other ingredients, release and approved uses can differ — ask a pharmacist before swapping.

Medicine passport: one printable page to show a pharmacist abroad

Details

Made byFSA Store Inc.
Active substanceLidocaine Hydrochloride
Used inPain, sleep, mood, epilepsy and the brain
Strength5 mg/mL
FormLiquid
RouteTopical
Packs237 mL in 1 BOTTLE
NDC81522-953

Source: NDC Directory · 2026-09-13 · not reviewed by a clinician

Source: US Food and Drug Administration, NDC Directory. Reuse terms: US government work (FDA).

Same active substance

These contain the same substance. That does not mean one can replace another — ask a pharmacist.