Pain Relief Tincture

Manufacturer
Henan Lingrui Pharmaceutical Co Ltd
Effective date
2015-03-19
Label type
HUMAN OTC DRUG LABEL
Version
3110
Source
full-release
Hydrated at
2026-05-31 22:42:02

Label at a glance#

ProductPain Relief Tincture
Active ingredientCAMPHOR (SYNTHETIC), MENTHOL
Label structure15 sections

Indications and uses

For the temporary relief of minor aches and pains of muscles and joints due to: simple backache arthritis strains bruises sprains

Dosage and administration

Adults and children 12 years of age and older: Apply to affected area three times a day, 2 - 5ml each time, a course of 15 days. Children 2 to 12 years of age and adults with compromised health: Use only under the guidance of a doctor. Children under 2 years of age: Do not use, consult a doctor. Refer to the above warnings: use otherwise than as directed may be dangerous.

Storage and handling

Keep container tightly closed. Store below 20 ℃ (68 ℉) in a dry area.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Camphor      5.0%

Menthol        1.3%

Purpose

OTC - PURPOSE SECTION

Camphor    External Analgesic

Menthol      External Analgesic

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches and pains of muscles and joints due to:

simple backache

arthritis

strains

bruises

sprains

Warnings

WARNINGS SECTION

For External Use Only.

Do not use

WARNINGS SECTION

on wounds

on irritated or damaged skin

if the appearance of this product has changed

in excess of 12 hours

if you have known hypersensitive to this product

otherwise than as directed

ASK A DOCTOR OR PHARMACIST BEFORE USE IF YOU ARE

OTC - ASK DOCTOR/PHARMACIST SECTION

pregnant

taking other medications

WHEN USING THIS PRODUCT

OTC - WHEN USING SECTION

avoid contact with the eye or mucous membranes

do not bandage tightly

supervise use by children

use caution if prone to allergic reactions

STOP USE AND ASK A DOCTOR IF

OTC - STOP USE SECTION

condition worsens

symptoms persist for more than 7 days

symptoms clear up and occur again within a few days

excessive irritation of the skin develops

when using for pain of arthritis

pain persists for more than 10 days

redness is present

in conditions affecting children under 12 years of age

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years of age and older: Apply to affected area three times a day, 2 - 5ml each time, a course of 15 days.

Children 2 to 12 years of age and adults with compromised health: Use only under the guidance of a doctor.
Children under 2 years of age: Do not use, consult a doctor.
Refer to the above warnings: use otherwise than as directed may be dangerous.

Other Information

STORAGE AND HANDLING SECTION

Keep container tightly closed.

Store below 20 ℃ (68 ℉) in a dry area.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

ANGELICA SINENSIS ROOT, LIGUSTICUM WALLICHII ROOT, SAFFLOWER, ZANTHOXYLUM PIPERITUM WHOLE, KAEMPFERIA GALANGA WHOLE, CINNAMON, GREEN PEPPERCORN, CHINESE RHUBARB ROOT, LONG PEPPER, GINGER, CLOVE, BORNEOL, ETHANOL

Drug Facts

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

cartoncarton

Questions or Comments?

OTC - QUESTIONS SECTION

E-mail: info@bjwellspring.com

Manufactured by

SPL UNCLASSIFIED SECTION

Henan Lingrui Pharmaceutical Co.; Ltd.

232 Xiang Yang Road, Xin County, Henan, China

Beijing Lingrui Wellspring Imp. & Exp. Co.; Ltd.

Overseas Exclusive Distribution

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1606183camphor 5 % / menthol 1.3 % Topical SolutionPSN3110
1606183camphor 50 MG/ML / menthol 13 MG/ML Topical SolutionSCD3110
1606183camphor 5 % / menthol 1.3 % Topical SolutionSY3110
1606183camphor 5 % / menthol 1.3 % Topical TinctureSY3110

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
42217-206-602020-01-31C16284748780-19d75b9d0-0640-f424-e053-dadaa90a57ceHenan Lingrui Pharmaceutical Co Ltd

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
42217-206-60Pain Relief Tincture60 mL in 1 BOTTLE, PLASTICTINCTURE603110

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
42217-206PAIN RELIEF TINCTURE (CAMPHOR, MENTHOL) TINCTURE [HENAN LINGRUI PHARMACEUTICAL CO LTD]3110Legacy NDC, 1 package rows20150319_27b01a94-e56f-4949-afe8-5ddcda282093.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CAMPHOR (SYNTHETIC)ACTIVE INGREDIENT5TJD82A1ET3110
MENTHOLACTIVE INGREDIENTL7T10EIP3A3110
CAMPHOR (SYNTHETIC)ACTIVE MOIETY5TJD82A1ET3110
MENTHOLACTIVE MOIETYL7T10EIP3A3110
ANGELICA SINENSIS ROOTINACTIVE INGREDIENTB66F4574UG3110
BORNEOLINACTIVE INGREDIENTM89NIB437X3110
CHINESE RHUBARB ROOTINACTIVE INGREDIENT5U759027OH3110
CINNAMONINACTIVE INGREDIENT5S29HWU6QB3110
CLOVEINACTIVE INGREDIENTK48IKT53213110
ETHANOL, 2-(BIS(2-METHYLPROPYL)PHENOXY)-INACTIVE INGREDIENTAUK0O5KW1Y3110
GINGERINACTIVE INGREDIENTC5529G5JPQ3110
GREEN PEPPERCORNINACTIVE INGREDIENT6G53L8ESRK3110
KAEMPFERIA GALANGA WHOLEINACTIVE INGREDIENTNU6Y8418BH3110
LIGUSTICUM WALLICHII ROOTINACTIVE INGREDIENTR81AD159QS3110
LONG PEPPERINACTIVE INGREDIENT2NMG4EA7B13110
SAFFLOWERINACTIVE INGREDIENT4VBL71TY4Y3110
ZANTHOXYLUM PIPERITUM WHOLEINACTIVE INGREDIENTY8IKP413383110

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
42217-20642217-206-60

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 4 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
GINGERGINGERC5529G5JPQSYRUP / ORAL0.05 ml/5mlExact identifier — unii candidate
2 equally ranked IID candidates
CINNAMONCINNAMON5S29HWU6QBELIXIR / ORAL10.5 mg/5mlExact identifier — unii candidate
2 equally ranked IID candidates
CINNAMONCINNAMON5S29HWU6QBCAPSULE / ORALNAExact identifier — unii candidate
2 equally ranked IID candidates
GINGERGINGERC5529G5JPQELIXIR / ORAL10 mg/5mlExact identifier — unii candidate
2 equally ranked IID candidates

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
447c97f3-b4a3-4a5d-9498-6e25f83665f727b01a94-e56f-4949-afe8-5ddcda2820932015-03-19WarningsExact identifier
spl id: 447c97f3-b4a3-4a5d-9498-6e25f83665f7
spl set id: 27b01a94-e56f-4949-afe8-5ddcda282093

Reported adverse events (FAERS/openFDA)#

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