Careland Pain Relief Cream
FDA Label NDC 75568-021

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Planet (anhui) Pharmaceutical Co., Ltd. for the product Careland Pain Relief (NDC 75568-021). 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 drug facts, active ingredient, purpose, uses:, warnings:, when using this product,, ask a health professional before use, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Drug Facts

Active Ingredient

Methyl Salicylate 20%

Menthol 10%

Purpose

Topical Analgesic

Uses:

For the temporary relief of minor aches and pains of muscles and joint

Warnings:

For external use only.

When Using This Product,

do not take by mouth or place in nostrils, apply to wounds or damaged skin. Use as directed

Ask A Health Professional Before Use

if you have sensitive skin or are pregnant or breastfeeding. Discontinue use if irritation occurs.

Keep Out Of Reach Of Children.

In case of accidental ingestion,get medical help or call Poison Control Center right away. Not for children 5 years or younger.

Directions:

Apply liberally to area of pain and massage until lotion is absorbed into the skin. Repeat 3-4 times daily. Store at 68'F to 77'F (20°C to 25°C)

Inactive Ingredients:

Capsaicin,2-Ethylhexyl palmitate, Aloe barbadensis (Aloe Vera),Carbomer,Cetearyl alcohol,Dimethylsilicone oil,Methylparaben, Phenoxyethanol,propyl glycol,Propylparaben,Purslane extract,Span 60,Triethanolamine,Tween 60,Water

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