Medical emergency?Emergency? Call 911. Nearest emergency roomsNearest ERs

Over-the-counter medicine · no prescription needed

Lidocaine and phenol

Purpose on the label: Topical Analgesic

Pain relief on the skin

Official FDA data, not advice

The label text is quoted exactly as the company filed it with the U.S. Food and Drug Administration (FDA), with a link to the official copy. The list of brands comes from the FDA NDC Directory.

This page is not medical advice. Read the label on your package, and ask a pharmacist or doctor if you are not sure a medicine is right for you, for your child, or with your other medicines.

If someone may have taken too much, call Poison Help: 1‑800‑222‑1222. In an emergency, call 911.

Quick answers

What is Lidocaine and phenol used for?
The Drug Facts label of Absorbine Jr Pro No Mess Roll-on Plus (Clarion Brands, LLC) lists these uses: for the temporary relief of pain.
Do I need a prescription for Lidocaine and phenol?
No. The products on this page are sold without a prescription (over the counter).
Is a store brand the same as the name brand?
Products listed together below have the same active ingredients, in the same amount and the same form, as registered with the FDA. Inactive ingredients (such as colors, flavors and fillers) and package sizes can differ. Compare the “Active ingredient” box on both packages, and ask a pharmacist if you are not sure.
Has Lidocaine and phenol been recalled?
No recall linked to these products appears in the FDA enforcement reports we use.

Drug Facts label

Every over-the-counter medicine must carry a “Drug Facts” box in the same order, set by FDA rules. Below is the label of one product for each common strength and form, quoted word for word. Your own package can differ (for example, children’s products have other directions): always follow the label on your package.

Absorbine Jr Pro No Mess Roll-on Plus · Clarion Brands, LLC

Lidocaine 4% · Phenol 1.5%, cream (topical)

Active ingredient

Lidocaine HCI 4%, Phenol 1.5%

Purpose

Topical Analgesic

Uses

for the temporary relief of pain

Warnings

Warnings For external use only.

Do not use

on large areas of the body, or on cut, irritated or swollen skin on puncture wounds for more than one week without consulting a doctor.

When using this product

use only as directed. Read and follow all directions and warnings on this label do not allow contact with the eyes and mucous membranes do not bandage tightly do not bandage or apply local heat such as heating pad or a medicated patch do not use with other topical analgesics.

Stop use and ask a doctor if

rash or irritation develops symptoms worsen or persist for more than 7 days or clear up and occur again within a few days. 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.

Directions

adults and children 2 years of age and older: apply to the affected area no more than 3 to 4 times daily children under 2 years of age; : ask a doctor

Inactive ingredients

aloe barbadensis leaf juice, aminomethyl propanol, bisabolol, cinnamomum camphora (camphor) leaf oil, fragrance, glycerin, hydroxyethylcellulose, mentha arvensis leaf oil, SD alcohol 40, water, zingiber oficinale (ginger)

Questions?

call 1-844-922-7672

— FDA label of Absorbine Jr Pro No Mess Roll-on Plus, Clarion Brands, LLC, effective December 23, 2025. See the official label on DailyMed →

Absorbine Jr. Pro Rollon · Clarion Brands, LLC

Lidocaine 4% · Phenol 1.5%, liquid (topical)

Active ingredient

Menthol 4.0%

Purpose

Topical Analgesic

Uses

For temporary relief of minor aches and pains of muscles and joints associated with: arthritis simple backache sprains strains bruises

Warnings

For external use only. Use only as directed. Flammable Keep away from fire, flame, sparks and heated surfaces. Tighten cap firmly.

When using this product

Avoid contact with the eyes Do not apply to wounds or damaged skin Do not bandage tightly

Stop use and ask a doctor if

Condition worsens or symptoms persist for more than 7 days or clear up and occur again within a few days. 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.

Directions

adults and children 2 years of age and older: apply to the affected area no more than 3 to 4 times daily children under 2 years of age; consult a doctor

Inactive ingredients

acetone, chloroxylene, FD&C blue #1, Iodine, plant extracts of calendula, echinacea, wormwood herb, potassium iodide, thymol, water, and wormwood oil

Questions?

Call 1-844-922-7672

— FDA label of Absorbine Jr. Pro Rollon, Clarion Brands, LLC, effective December 28, 2025. See the official label on DailyMed →

ABSORBINE jr. · Clarion Brands, LLC

Lidocaine hydrochloride 4% · Phenol 1.5%, spray (topical)

Active ingredient

Purpose Lidocaine HCL 4%, Phenol 1.5% Topical anesthetic

Uses

for the temporary relief of pain

Warnings

For external use only Flammable do not use near heat or flame or while smoking avoid long term storage above 104ºF (40ºC) do not puncture or incinerate container. Contents under pressure

Do not use

on large areas of the body or on cut, irritated or swollen skin on puncture wounds for more than one week without consulting a doctor

When using this product

avoid spraying on face avoid inhalation of spray use only as directed. Read and follow all directions and warning on this label do not allow contact with the eyes and mucous membranes do not bandage or apply local heat such as heating pad or a medicated patch do not use with other topical analgesics

Stop use and ask a doctor if

symptoms worsen or persist for more than 7 days or clear up and occur again within a few days rash or irritation develops

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.

Directions

adults and children 2 years of age and older: apply to the affected area no more than 3 to 4 times daily children 2 years of age: ask a doctor

Inactive ingredients

alcohol denat., aloe barbadersis leaf extract, bisabolol, butane, camphor, carthamus tinctorius (safflower) seed oil, fragrance, isobutane, isopropyl myristate, mentha arvensis leaf oil, phenoxyethanol, water, zingiber offcinale (ginger) root extract

Questions?

call 1-844-923-7837

— FDA label of ABSORBINE jr., Clarion Brands, LLC, effective December 23, 2025. See the official label on DailyMed →

This page is not medical advice. Read the label on your package, and ask a pharmacist or doctor if you are not sure a medicine is right for you, for your child, or with your other medicines.

Same medicine, other brands

Each group lists the products that have exactly the same active ingredients, in the same amount and form, as registered with the FDA (NDC Directory). A store brand in the same group has the same medicine as the name brand; inactive ingredients, flavors and package sizes can differ. Each product links to its own official label.

Lidocaine 4% · Phenol 1.5% · cream (topical) · 2 products

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Absorbine Jr Pro Cream Clarion Brands, LLC DailyMed
Absorbine Jr Pro No Mess Roll-on Plus Clarion Brands, LLC DailyMed
Lidocaine 4% · Phenol 1.5% · liquid (topical) · 1 product

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
Absorbine Jr. Pro Rollon Clarion Brands, LLC DailyMed
Lidocaine hydrochloride 4% · Phenol 1.5% · spray (topical) · 1 product

Drug Facts for this strength and form ↑

Brand or product nameCompany on the labelLabel
ABSORBINE jr. Clarion Brands, LLC DailyMed

Companies that sell this medicine

The company named on the package (maker or distributor), as listed in the FDA NDC Directory, with its number of over-the-counter products of this medicine.

  • Clarion Brands, LLC4 products

Recalls

No recall linked to these products (by their NDC code or label) appears in the FDA enforcement reports.

Sources

  1. Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  2. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
  4. FDA rule for the Drug Facts label (21 CFR 201.66)

Only medicines marketed under FDA rules for nonprescription drugs (an FDA monograph or an FDA approval) are listed. Homeopathic products are not listed: the FDA does not evaluate them for safety or effectiveness.

Report an error → · Information for medicine makers