Pure InflaMedix Natural Pain Relief Cream

Manufacturer
Nutragen Health Innovations, Inc.
Effective date
2018-01-11
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:05:10

Label at a glance#

ProductPure InflaMedix Natural Pain Relief
Active ingredientMENTHOL
Label structure8 sections

Indications and uses

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

Dosage and administration

use only as directed adults and children two-years of age or older:  apply to affected area not more than three to four times daily children under two-years of age:  consult a physician

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 3.00%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

temporary relief of minor aches and pains of the muscles and joints associated with:

- arthritis    - simple backache   - sprains    - bruises    - strains

​Warnings

WARNINGS SECTION

​For external use only.

OTC - STOP USE SECTION

  • avoid contact with eyes.
  • if symptoms persist for more than seven days, discontinue use and consult a physician.

OTC - DO NOT USE SECTION

  • do not apply to wounds, damaged or open skin.
  • do not bandage tightly

If pregnat or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a healthcare professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental overdose, get medical help or contact a Poison Control Center immediately (800)222-1222

Directions

DOSAGE & ADMINISTRATION SECTION

  • use only as directed
  • adults and children two-years of age or older:  apply to affected area not more than three to four times daily
  • children under two-years of age:  consult a physician

​Other information

SPL UNCLASSIFIED SECTION

  • Store at room temperature

​Inactive ingredients

INACTIVE INGREDIENT SECTION

Organic Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Organic Arnica Montana Flower Extract, Organic Boswellia Carteria (Frankincense) Oil, Ceteryl Olivate, Organic Curcuma Longa (Turmeric) Oil, Emul Oil, Organic Eucalyptus Globulus Oil, Glycerin, Glyceryl Caprylate, Glyceryl stearate, Glyceryl Undecylenate, Organic Hellanthus Annuus (Sunflower) Oil, Methylsulfonylmethana (MSM), Sorbitan Olivate, Organic Symphytum Officinale (Comfrey) Extract, Xanthan Gum, Organic Zingiber Officinale (Ginger) Root Oil.

​Questions?

OTC - QUESTIONS SECTION

call toll free 877-417-PURE (7873)

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72016-14072016-140-03

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
074b2822-cc0a-d614-e063-6394a90a266588307acf-371c-4b98-be14-949bd1ab33d62023-10-09WarningsExact identifier
spl set id: 88307acf-371c-4b98-be14-949bd1ab33d6

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.