KWIK-MOVING

Manufacturer
N. N. IMPEX | ECLAT PHARMA & AEROSOLS PVT LTD
Effective date
2021-03-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:38:43

Label at a glance#

ProductKWIK-MOVING
Active ingredientEUCALYPTUS OIL, MENTHOL, METHYL SALICYLATE, CAPSICUM OLEORESIN
Label structure8 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

Capsicum oleoresin 0.02% ,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. Irritation 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. Avoid spraying on face. Avoid inhalation of spray.

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

Extremely Flammable

do not use near heat or flame or while smoking. Avoid long term storage above 104 °F (40 °C)do not puncture or incinerate. Contents
under pressure. Do not store at temperatures above 120 °F (49 °C).

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 over 12 years : spray affected area up to 4 times daily. product will dry quickly on its own, and
does not need to be rubbed in. Children under 12 years : ask a doctor

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

Isopropyl alcohol, propellant, propylene glycol, turpentine oil.

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2529761capsicum oleoresin 0.02 % / eucalyptus oil 2 % / menthol 5 % / menthol salicylate 15 % Topical SprayPSN1
2529761Capsicum oleoresin 0.2 MG/ML / Eucalyptus oil 20 MG/ML / menthol 50 MG/ML / methyl salicylate 150 MG/ML Topical SpraySCD1
2529761capsicum oleoresin 0.02 % / eucalyptus oil 2 % / menthol 5 % / menthol salicylate 15 % Topical SpraySY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
473d070d-1c38-488e-b991-c4d1bf45aab8Product name120210201

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73640-020-012022-07-29C16284748780-1e4f33bdf-a6c6-d8a0-e053-dadaa90a6e4ed7b29a1d-ef20-4332-8c3a-309d8fed6fd6

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73640-020-01KWIK-MOVING150 mL in 1 BOTTLE, SPRAYSPRAY1501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73640-020KWIK-MOVING (EUCALYPTUS, MENTHOL, METHYL SALICYLATE, CAPSICUM OLEORESIN) SPRAY [N. N. IMPEX]1Legacy NDC, 1 package rows20210303_d7b29a1d-ef20-4332-8c3a-309d8fed6fd6.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73640-02073640-020-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
bc80a337-31de-85f6-e053-2995a90a2663d7b29a1d-ef20-4332-8c3a-309d8fed6fd62021-03-01WarningsExact identifier
spl id: bc80a337-31de-85f6-e053-2995a90a2663
spl set id: d7b29a1d-ef20-4332-8c3a-309d8fed6fd6

Reported adverse events (FAERS/openFDA)#

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