DRAWYUM Pain Relief Gel-Patch

Manufacturer
Jiangxi Hemei Pharmaceutical Co., Ltd
Effective date
2026-01-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
monthly-update
Hydrated at
2026-06-03 17:51:20

Label at a glance#

ProductDRAWYUM Pain Relief Gel-Patch
Active ingredientLIDOCAINE
Label structure12 sections

Dosage and administration

adults and children over 12 years. ▆remove backing from patch by firmly grasping both ends and gently pulling until backing separate in middle ▆carefully remove smaller portion of backing from patch and apply exposed portion of patch to affected area ▆once exposed portion of patch is positioned, carefully remove remaining backing to completely apply patch to affected area ▆Wear one patch for up to 8 hours. ▆Repeat...

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4%

Purpose

OTC - PURPOSE SECTION

Pain Relief

Use

INDICATIONS & USAGE SECTION

▆temporarily relieves minor pain associated with: ▆arthritis ▆simple backache▆bursitis ▆tendonitis ▆muscle strains ▆sprains▆bruises ▆cramps

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

▆use only as directed. Read and follow all directions and warnings on this carton. ▆avoid contact with eyes and mucous membranes ▆rare cases of serious burns have been reported with products of this type ▆ do not apply to wounds or damaged skin, broken or irritated skin ▆do not bandage tightly or apply local heat (such as heating pads) to the area of use ▆ A transient burning sensation may occur upon application but usually disappears within a few days.

When Using

OTC - WHEN USING SECTION

▆use only as directed. Read and follow all directions and warnings on this carton. ▆avoid contact with eyes and mucous membranes ▆rare cases of serious burns have been reported with products of this type ▆ do not apply to wounds or damaged skin, broken or irritated skin ▆do not bandage tightly or apply local heat (such as heating pads) to the area of use ▆ A transient burning sensation may occur upon application but usually disappears within a few days.

Stop Use

OTC - STOP USE SECTION

▆condition worsens ▆redness is present ▆irritation develops▆symptoms persist for more than 7 days or clear up and occur again within a few dsys ▆you experience signs of skin injury, such as pain, swelling, or blistering where the product was applied If pregnant or breast-feeding. ask a health professional before use

Ask Doctor

OTC - ASK DOCTOR SECTION

▆condition worsens ▆redness is present ▆irritation develops▆symptoms persist for more than 7 days or clear up and occur again within a few dsys ▆you experience signs of skin injury, such as pain, swelling, or blistering where the product was applied

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. lf swallowed, get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

adults and children over 12 years. ▆remove backing from patch by firmly grasping both ends and gently pulling until backing separate in middle ▆carefully remove smaller portion of backing from patch and apply exposed portion of patch to affected area ▆once exposed portion of patch is positioned, carefully remove remaining backing to completely apply patch to affected area ▆Wear one patch for up to 8 hours. ▆Repeat if needed, but do not use more than 3 times daily. children 12 years or younger: ask a doctor

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, aluminym hvdroxide, cellulose gum, glvcerin, isopropyl myristate, nonoxynol-30, polyacrylic acid,polysorbate 80, sodium polvacrvlate, sorbitan sesauioleate,Starch, talc, tartaric acid,titanium dioxide

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

44

DailyMed Product Concepts#

Product concept, Relation, Version table
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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84010-24384010-243-01

Ingredients#

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DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Source Document#

Source XML

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
4a45e19d-dc4b-ed8b-e063-6394a90a725e479c767b-d97b-6974-e063-6294a90af3ef2026-02-07WarningsExact identifier
spl set id: 479c767b-d97b-6974-e063-6294a90af3ef

Reported adverse events (FAERS/openFDA)#

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