FDA.reportPublic FDA data

Pain Relief Cream

Manufacturer
Zhejiang Apeloa Kangyu Pharmaceutical Co., Ltd.
Effective date
2016-04-05
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-02 01:27:40

Label at a glance#

ProductPain Relief Cream
Active ingredientCAMPHOR (NATURAL)
Label structure8 sections

Label contents#

Full prescribing information#

OTC - PURPOSE SECTION

-External Analgesic

-Topical Analgesic

-Pain relieving cream

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Children under 2 years of age: consult a doctor

INDICATIONS & USAGE SECTION

Temporarily relieves minor aches and pains of muscles and joints associated with:

-simple backache

-arthritis

-strains

-bruises

-sprains

WARNINGS SECTION

Do Not Use:

-on wounds

-on irritated or damaged skin

-otherwise than as directed

DOSAGE & ADMINISTRATION SECTION

Adults and children 3 years of age and older: apply 3 to 4 drops of medicated oil to the affected area 1 to 2 times daily. After appling the product, a warm pad may be placed on the affected area for 10 minutes and then massaged as shown in the illustrations.

INACTIVE INGREDIENT SECTION

-Yellow Vaseline

-Wool Grease

-Liquid Paraffin

-Stearic Acid

-Glycerol

-Triethanolamine

-Ethylparaben

-Dimethyl Sulfoxide

-Radix Illcis Pubescentis

-Cortex Araliae

-Pheretima

-Herba Hedyotis Chrysotricae

-Radix Pini Massonianae

-Sophorae Flavescentis Radix

-Drynariae Rhizoma

-Radix Adinae Rubellae

-Radix Cudraniae Cochinchinensis

-Root from Itea Oblonga Hand.-Mazz

-Root from Syzygium Grijsii (Hance) Merr.Et

-Perry & Root from Ampelopsis Sinica (MIQ) W.T. Wang & Root from Ormosia Henryi Prain & Cuscuta Japonica Choisy

OTC - ACTIVE INGREDIENT SECTION

Camphor 1%

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Pain Relief CreamPain Relief Cream

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
66653-100-012024-12-19C16284748780-1ba0f9c33-4aa2-a910-e053-dadaa90a0b852fbfc4ac-75a5-6e28-e054-00144ff8d46c
66653-100-012021-01-29C16284748780-1ba0f9c33-4aa2-a910-e053-dadaa90a0b852fbfc4ac-75a5-6e28-e054-00144ff8d46c

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66653-10066653-100-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 matching rows.

Name, UNII, Kind table
NameUNIIKind
SOPHORA FLAVESCENS ROOTIYR6K8KQ5KIACT
MACLURA COCHINCHINENSIS ROOT3WTU9E1VPUIACT
CAMPHOR (NATURAL)N20HL7Q941ACTIB
LANOLIN7EV65EAW6HIACT
MINERAL OILT5L8T28FGPIACT
ETHYLPARABEN14255EXE39IACT
ILEX PUBESCENS ROOTV5V22LFX73IACT
GLYCERINPDC6A3C0OXIACT
TROLAMINE9O3K93S3TKIACT
DIMETHYL SULFOXIDEYOW8V9698HIACT
ARALIA CHINENSIS WHOLE4048809221IACT
AMPELOPSIS GLANDULOSA VAR. BREVIPEDUNCULATA FRUITY6SZ1HB5NGIACT
PHERETIMA ASPERGILLUM1842H27PGAIACT
PETROLATUM4T6H12BN9UIACT
STEARIC ACID4ELV7Z65APIACT
OLDENLANDIA DIFFUSA291PPU5K9IIACT
PINUS MASSONIANA LEAFOFD5T4515TIACT
DRYNARIA FORTUNEI ROOT731W842X8QIACT
ADINA RUBELLA WHOLE1S210XS3BZIACT

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
296d362e-5535-2f40-e063-6294a90a06ca2fbfc4ac-75a5-6e28-e054-00144ff8d46c2024-12-16WarningsExact identifier
spl set id: 2fbfc4ac-75a5-6e28-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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