osteodin-z

Manufacturer
Adven Biotech Private Limited
Effective date
2016-02-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:07:30

Label at a glance#

Productosteodin-z
Active ingredientHYPERICUM PERFORATUM, RUTA GRAVEOLENS WHOLE, BELLIS PERENNIS, TOXICODENDRON PUBESCENS LEAF, MENTHOL
Label structure7 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Adults: Apply externally twice daily to properly cleaned & dried affected portion.

Children under 18 years: Please consult physician.

WARNINGS SECTION

If symptons persist or worsen, a physician should be consulted. Keep out of reach of children. Do not use, if known sentivity to any of its ingredients exists. In case of emergency, contact a medical professional or posion control center immediately. For external use only. Replace cap tightly.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

INACTIVE INGREDIENT SECTION

Vaseline base

OTC - PURPOSE SECTION

Relieves arthritis pain

Relieves joint pain

Relieves pain

OTC - ACTIVE INGREDIENT SECTION

Rhus toxicondendron, Hypericum perforatum, Ruta graveolens, Bellis pernnis, Menthol

INDICATIONS & USAGE SECTION

For the relief of joins pain, ligaments & tendons pain, Rheumatic pain, Sciatica, Neuralgia, Cramps in calves, Sprains, Muscular soreness.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Osteodin z OintmentOsteodin z Ointment

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69825-003-022020-01-31C16284748780-19d75b9cf-fc4d-f424-e053-dadaa90a57ce2ae64e09-670e-6f7f-e054-00144ff8d46c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69825-003-01osteodin-z30 g in 1 TUBEOINTMENT301
69825-003-02osteodin-z1 in 1 BOXOINTMENT11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69825-003OSTEODIN-Z (RHUS TOXICONDENDRON, HYPERICUM PERFORATUM, RUTA GRAVEOLENS, BELLIS PERRNNIS, METHYL SALICYLATE, MENTHOL) OINTMENT [ADVEN BIOTECH PRIVATE LIMITED]1Legacy NDC, 2 package rows20160208_2ae64e09-670e-6f7f-e054-00144ff8d46c.zip

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
69825-00369825-003-01, 69825-003-02

Ingredients#

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

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

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
2ae64e09-670f-6f7f-e054-00144ff8d46c2ae64e09-670e-6f7f-e054-00144ff8d46c2016-02-08WarningsExact identifier
spl id: 2ae64e09-670f-6f7f-e054-00144ff8d46c
spl set id: 2ae64e09-670e-6f7f-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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