Nulido
FDA Label NDC 53149-2100

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by All Pharma Llc for the product Nulido (NDC 53149-2100). 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 ingedients, inactive ingredient, warnings, keep out of reach of children, when using this product, ask your doctor before use if, uses, purpose, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingedients

Each milliliter contains
 Active Ingredient Purpose
 Lidocaine Hydrochloride 4.0% Topical Anesthetic
 Menthol 1.0% Topical Anesthetic

Inactive Ingredient

Carbomer copolymer type b, Isopropyl Alcohol, water, trolamine

Warnings

For external use only.

Keep Out Of Reach Of Children

If swallowed, get medical help or contact a Poison Control Center right away. Package not child resistant.

When Using This Product

■ avoid contact with eyes, genitals, and other mucous membranes. If eye contact occurs, rinse thoroughly with water.
■ do not use on open wounds, cuts, damaged or infected skin
■ do not use With a bandage or a heating pad

Ask Your Doctor Before Use If

■ you are allergic to any ingredients
■ you are pregnant or breast-feeding

Uses

Temporarily relieves minor aches and muscle pains associated with:


■ arthritis

■ simple back pain

■ strains

■ muscle soreness

Purpose

Temporarily relieves minor aches and muscle pains associated with:

■ arthritis
■ simple back pain
■ strains
■ muscle soreness

Dosage & Administration

Apply to the affected area.
 Adults and children 12 years and older

 Apply to the affected area.
Product may be used as necessary, but should not
be used more than four times per day.


Wash hands immediately afterwards.

Children under 2Ask a doctor

Other Information

■ avoid storing product in direct sunlight
■ protect product from excessive moisture
■ store at 67-77°F (19-25°C)

Stop Use And Ask Doctor

■ if condition worsens or symptoms persist for more than 7 days
■ if excessive skin irritation occurs

Label Image

Manufactured by:
All Pharma, LLC
Hialeah, FL 33016
www.allpharmallc.com
Made in the U.S.A.

Nulido Label (Labelimage)

Nulido Label (Labelimage)

* Please review the disclaimer below.