FDA.reportPublic FDA data

SANAR - POMADA DE ARNICA

Manufacturer
SANVALL ENTERPRISES, INC | CHEMCO CORPORATIOM | CHEMCO CORPORATION
Effective date
2022-06-29
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:55:29

Label at a glance#

ProductSANAR - POMADA DE ARNICA WHITE
Active ingredientCAMPHOR (NATURAL)
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Camphor ……………………………………………………………………………………….………………... 1.%

OTC - PURPOSE SECTION

Pain Relieving

INDICATIONS & USAGE SECTION

Aid for temporary local relief of minor pain in muscles or joints.

WARNINGS SECTION

For external use only. Avoid contact with eyes.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

Adults and Children over 12 years: Apply generously to affected area. Massage until thoroughly absorbed. Repeat as necessary, but not more than 3 times daily. Children under 12 years: Consult a doctor.

INACTIVE INGREDIENT SECTION

Petrolatum, Cetyl Alcohol, Menthol, Methyl Salicylate, Arnica Montana Flower Extract.

OTC - DO NOT USE SECTION

DO NOT * Use on wounds or damaged skin. * Bandage tightly

OTC - ASK DOCTOR SECTION

Condition worsens or if symptoms persist for more than 7 days or clear up and occur.

OTHER SAFETY INFORMATION

OTHER INFORMETION • Store tightly closed in a dry place at controlled room temperature between 59°-77° F (15°-25° C). • Processed under the highest standards of quality assurance and Good Manufacturing Practices.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

2 oz2 oz

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73386-142-412024-11-13C16284748780-11030e365-3aed-111a-e063-dadaa90a10e273386-142-41
73386-142-412024-01-30C16284748780-11030e365-3aed-111a-e063-dadaa90a10e273386-142-41

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73386-14273386-142-41

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
MENTHOL, UNSPECIFIED FORML7T10EIP3AIACT
METHYL SALICYLATELAV5U5022YIACT
CAMPHOR (NATURAL)N20HL7Q941ACTIB
PETROLATUM4T6H12BN9UIACT
ARNICA MONTANA FLOWEROZ0E5Y15PZIACT
CETYL ALCOHOL936JST6JCNIACT

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
26cf264b-f68a-5691-e063-6394a90a8ab49fa50b4e-658e-e0bf-e053-2a95a90a82a92024-11-13WarningsExact identifier
spl set id: 9fa50b4e-658e-e0bf-e053-2a95a90a82a9

Reported adverse events (FAERS/openFDA)#

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