KWIK-MOVING

Manufacturer
N. N. IMPEX | ECLAT PHARMA & AEROSOLS PVT LTD
Effective date
2021-02-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:38:14

Label at a glance#

ProductKWIK-MOVING
Active ingredientEUCALYPTUS OIL, MENTHOL, METHYL SALICYLATE
Label structure9 sections

Indications and uses

For temporary relief of minor aches and pains of muscles and joints due to: simple backaches, bruises, sprains, arthritis

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Eucalyptus Oil 2% , Menthol 5% ,Methyl salicylate 15%

Purpose

OTC - PURPOSE SECTION

External Analgesic

Warning

WARNINGS SECTION

For external use only.

Allergy alert:If prone to allergic reaction from aspirin or salicylates, consult a doctor before use.


Stop use and ask a doctor if condition
 worsens or if symptoms persist for more than 7 days or clear up and occurs again within a few days. Redness is present. Excessive irritation of the skin develops.

When using this product

Use only as directed. Avoid contact with the eyes or mucous membranes. Do not apply on wounds and damaged skin. Do not bandage tightly. Do not use with heating pad.

If pregnant or breast-feeding, ask a health professional before use.

Uses

INDICATIONS & USAGE SECTION

For temporary relief of minor aches and pains of muscles and joints due to: simple backaches, bruises, sprains, arthritis

Direction

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years and older: apply to the affected area and massage gently not more than 3 to 4 times daily.
Children under 12 years of age :consult a physician.

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.

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Light liquid paraffin, microcrystalline wax, paraffin wax, turpentine oil

Other information

SPL UNCLASSIFIED SECTION

Store at room temperature.

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73640-019-012022-07-29C16284748780-1e4f33bdf-b32b-d8a0-e053-dadaa90a6e4e42190b8a-2c1a-4cdf-8752-120b5dee3b94
73640-019-022022-07-29C16284748780-1e4f33bdf-b32b-d8a0-e053-dadaa90a6e4e42190b8a-2c1a-4cdf-8752-120b5dee3b94

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73640-019-01KWIK-MOVING50 g in 1 TUBEOINTMENT501
73640-019-02KWIK-MOVING100 g in 1 TUBEOINTMENT1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73640-019KWIK-MOVING (EUCALYPTUS, MENTHOL, METHYL SALICYLATE) OINTMENT [N. N. IMPEX]1Legacy NDC, 2 package rows20210220_42190b8a-2c1a-4cdf-8752-120b5dee3b94.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73640-01973640-019-01, 73640-019-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
bbb53552-fd40-a688-e053-2995a90a2a6642190b8a-2c1a-4cdf-8752-120b5dee3b942021-02-19WarningsExact identifier
spl id: bbb53552-fd40-a688-e053-2995a90a2a66
spl set id: 42190b8a-2c1a-4cdf-8752-120b5dee3b94

Reported adverse events (FAERS/openFDA)#

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