Natural Pain Relief Foot Cream

Manufacturer: Tripak Pharmaceuticals
Effective date: 2023-12-18
Label type: HUMAN OTC DRUG LABEL
Version: 5
Source: full-release
Hydrated at: 2026-06-01 00:04:52

Label at a glance#

ProductNatural Pain Relief Foot Cream

Active ingredientCAMPHOR (NATURAL)

Label structure7 sections

Indications and uses

Uses For the temporary relief of pain.

Dosage and administration

Directions 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.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient Purpose

Camphor 3%..............................................................................Pain Relieving cream

Purpose

OTC - PURPOSE SECTION

Natural Pain Relieving Cream

Uses

INDICATIONS & USAGE SECTION

Uses

For the temporary relief of pain.

Warnings

WARNINGS SECTION

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 agai within a few days, discontinue use of this product and consult a doctor.

Do Not Use

OTC - DO NOT USE SECTION

Do not use on broken or irritated skin.

Stop Use

OTC - STOP USE SECTION

Stop use and ask a doctor if skin irritation develops.

If pregnant or breastfeeding

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding, ask a health professional before use.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children, in case of overdose, get medical help or contact a poison control center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions

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.

Other Information

OTHER SAFETY INFORMATION

Other Information

Shake well prior to use.

Store below 30C/86F

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Arnica montana extract, Anhydrous citric acid, frankincense oil, cajuput oil, camphor (natural) decyl glucoside, citric acid, clove oil, decyl polyglucoside, eucalyptus oil, glycerin, peppermint oil, potassium sorbate, purified water, sorbitan oleate, rosemary oil

Natural Foot Cream Box

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label 82309-033-01 Label

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

82309-33-02 Box

Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1802553	camphor 3 % Topical Cream	PSN	5
1802553	camphor 30 MG/ML Topical Cream	SCD	5
1802553	camphor 3 % Topical Cream	SY	5

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
82309-033-02	2025-01-30	C162847	48780-1	f386c64a-315f-0266-e053-dadaa90a7c1a	Pain Relief Foot Cream
82309-033-02	2023-12-18	C162847	48780-1	f386c64a-315f-0266-e053-dadaa90a7c1a	Pain Relief Foot Cream
82309-033-02	2023-01-30	C162847	48780-1	f386c64a-315f-0266-e053-dadaa90a7c1a	Pain Relief Foot Cream

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
82309-033-01	Natural Pain Relief Foot Cream	50 g in 1 TUBE	CREAM	50		5
82309-033-02	Natural Pain Relief Foot Cream	1 in 1 BOX	CREAM	1		5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
82309-033	NATURAL PAIN RELIEF FOOT CREAM (CAMPHOR) CREAM [TRIPAK PHARMACEUTICALS]	5	Legacy NDC, 2 package rows	20231219_d2183ea0-0bdd-08eb-e053-2995a90ac71c.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 17 matching rows.

Natural Pain Relief Foot Cream
camphor
PEG-6 SORBITAN OLEATE
GLYCERIN
ROSEMARY OIL
EUCALYPTUS OIL
POTASSIUM SORBATE
ANHYDROUS CITRIC ACID
WATER
CAMPHOR (NATURAL)
DECYL GLUCOSIDE
PEPPERMINT OIL
PEPPERMINT
FRANKINCENSE OIL
ARNICA MONTANA
CAJUPUT OIL
CLOVE OIL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
82309-033	82309-033-01, 82309-033-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
PEG-6 SORBITAN OLEATE	58O7V09UCI	IACT
GLYCERIN	PDC6A3C0OX	IACT
ROSEMARY OIL	8LGU7VM393	IACT
EUCALYPTUS OIL	2R04ONI662	IACT
POTASSIUM SORBATE	1VPU26JZZ4	IACT
ANHYDROUS CITRIC ACID	XF417D3PSL	IACT
WATER	059QF0KO0R	IACT
CAMPHOR (NATURAL)	N20HL7Q941	ACTIB
DECYL GLUCOSIDE	Z17H97EA6Y	IACT
PEPPERMINT OIL	AV092KU4JH	IACT
FRANKINCENSE OIL	67ZYA5T02K	IACT
ARNICA MONTANA	O80TY208ZW	IACT
CAJUPUT OIL	J3TO6BUQ37	IACT
CLOVE OIL	578389D6D0	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
0cca45e4-0549-5fbb-e063-6294a90a8098			d2183ea0-0bdd-08eb-e053-2995a90ac71c	2023-12-18	Warnings	Exact identifier spl id: 0cca45e4-0549-5fbb-e063-6294a90a8098 spl set id: d2183ea0-0bdd-08eb-e053-2995a90ac71c

Reported adverse events (FAERS/openFDA)#

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