FDA.reportPublic FDA data

Back Pain Relieving Oil

Manufacturer
International Nature Nutraceuticals | Chan Yat Hing Medicine Fty
Effective date
2013-10-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:37:15

Label at a glance#

ProductBack Pain Relieving Oil
Active ingredientCAMPHOR (NATURAL), METHYL SALICYLATE, MENTHOL
Label structure10 sections

Indications and uses

The temporary relief of minor aches and pains of muscles and joints due to: 暫時舒緩因下列症狀引致的肌肉和 關節酸痛:。Simple backache 一般腰腿痛。Sprains 扭傷。 Bruises 瘀傷。Arthritis 關節炎

Dosage and administration

Adults and children 6 years of age and older: Apply to affected area not more than 3~4 times daily. Children under 6 years of age: Do not use, consult a doctor. 成人及六歲以上的兒童, 塗在患處緩和地旋轉直至完全滲透,每日 3-4次. 六歲以下的小童請諮詢醫生.

Label contents#

Full prescribing information#

Active Ingredients:

OTC - ACTIVE INGREDIENT SECTION

Camphor- 9%

Methyl Salicylate- 17%

Menthol 11%

Uses:

OTC - PURPOSE SECTION

The temporary relief of minor aches and pains of

muscles and joints due to: 暫時舒緩因下列症狀引致的肌肉和

關節酸痛:。Simple backache 一般腰腿痛。Sprains 扭傷。

Bruises 瘀傷。Arthritis 關節炎

Warning:

WARNINGS SECTION

For external use only

Do Not Use:

OTC - DO NOT USE SECTION

If pregnant 孕婦禁用。If allergic to any

of the ingredients 如對任何成份過敏,不要使用。

Avoid contact with the eyes 避免接觸眼睛.

Stop use and consult a doctor if:

OTC - STOP USE SECTION

Condition worsens 情況變壞。Symptoms persist for more then

7 days or clear up and occur again within a few days 症狀持續

七天以上或好轉數天後再復發。Excessive irritation of the skin

develops 皮膚出現極度過敏或發炎。Do not apply to wound or

damaged skin 不要用於傷口或破損的皮膚。Do not bandage

tightly 不要包紮過緊.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, contact a doctor

or poison control center immediately 存放在兒童觸摸不到

之處,如不慎意外吞下,請馬上和醫生或毒物控制中心聯絡.

Directions:

DOSAGE & ADMINISTRATION SECTION

Adults and children 6 years of age and older: Apply to

affected area not more than 3~4 times daily. Children

under 6 years of age: Do not use, consult a doctor.

成人及六歲以上的兒童, 塗在患處緩和地旋轉直至完全滲透,每日

3-4次. 六歲以下的小童請諮詢醫生.

Other Information:

INDICATIONS & USAGE SECTION

Keep bottle tightly closed, store in a cool and dry place

保持瓶子緊閉,貯存在陰涼乾燥之處.Do not use if seal is

broken 如封蓋有損壞,不要使用.Keep

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Panax Notoginseng Root 田七.

Angelica Sinensis Root 當歸.Scutellaria Baicalensis Root 黃苓

Myrrh 沒藥,Frankincense 乳香,

Citronella Oil 香茅油,Notopterygium Incisum Root 薑活

Eucalyptus Oil桉葉油

Dragon’s Blood 血竭,

Angelica Biserrata root 獨活

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

packagepackage

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1441310camphor 9 % / menthol 11 % / methyl salicylate 17 % Topical OilPSN1
1441310camphor 90 MG/ML / menthol 110 MG/ML / methyl salicylate 170 MG/ML Topical OilSCD1
1441310camphor 9 % / menthol 11 % / methyl salicylate 17 % Topical OilSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51367-014-402019-11-27C16284748780-19855e2a2-38a0-60a7-e053-dbdaa90a05bdDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51367-014-40Back Pain Relieving Oil1 in 1 BOTTLEOIL11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51367-014BACK PAIN RELIEVING OIL (CAMPHOR, METHYL SALICYLATE, MENTHOL) OIL [INTERNATIONAL NATURE NUTRACEUTICALS]1Legacy NDC, 1 package rows20131021_91bf3641-e83d-49e9-9b53-ce7c37452811.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CAMPHOR (NATURAL)ACTIVE INGREDIENTN20HL7Q9411
MENTHOLACTIVE INGREDIENTL7T10EIP3A1
METHYL SALICYLATEACTIVE INGREDIENTLAV5U5022Y1
CAMPHOR (NATURAL)ACTIVE MOIETYN20HL7Q9411
MENTHOLACTIVE MOIETYL7T10EIP3A1
SALICYLIC ACIDACTIVE MOIETYO414PZ4LPZ1
ANGELICA BISERRATA ROOTINACTIVE INGREDIENTOJ90180B221
ANGELICA SINENSIS ROOTINACTIVE INGREDIENTB66F4574UG1
CITRONELLA OILINACTIVE INGREDIENTQYO8Q067D01
DRAGON'S BLOODINACTIVE INGREDIENTM3YJ2C28IC1
EUCALYPTUS OILINACTIVE INGREDIENT2R04ONI6621
FRANKINCENSEINACTIVE INGREDIENTR9XLF1R1WM1
MYRRHINACTIVE INGREDIENTJC71GJ1F3L1
NOTOPTERYGIUM INCISUM ROOTINACTIVE INGREDIENT5Z2WW4J6RI1
PANAX NOTOGINSENG ROOTINACTIVE INGREDIENTGQX1C1175U1
SCUTELLARIA BAICALENSIS ROOTINACTIVE INGREDIENT7J95K7ID2S1

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51367-01451367-014-40

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
PANAX NOTOGINSENG ROOTGQX1C1175UIACT
DRAGON'S BLOODM3YJ2C28ICIACT
ANGELICA SINENSIS ROOTB66F4574UGIACT
SCUTELLARIA BAICALENSIS ROOT7J95K7ID2SIACT
MYRRHJC71GJ1F3LIACT
FRANKINCENSER9XLF1R1WMIACT
ANGELICA BISERRATA ROOTOJ90180B22IACT
CITRONELLA OILQYO8Q067D0IACT
NOTOPTERYGIUM INCISUM ROOT5Z2WW4J6RIIACT
EUCALYPTUS OIL2R04ONI662IACT
CAMPHOR (NATURAL)N20HL7Q941ACTIB
METHYL SALICYLATELAV5U5022YACTIB
MENTHOLL7T10EIP3AACTIB

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 · 1 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
EUCALYPTUS OILEUCALYPTUS OIL2R04ONI662SYRUP / ORALNAExact identifier — unii candidate

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
566ddf02-c8df-4217-aa60-767010a8e2be91bf3641-e83d-49e9-9b53-ce7c374528112013-10-20WarningsExact identifier
spl id: 566ddf02-c8df-4217-aa60-767010a8e2be
spl set id: 91bf3641-e83d-49e9-9b53-ce7c37452811

Reported adverse events (FAERS/openFDA)#

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