Walgreens Pain Relieving with Turmeric

Manufacturer
Walgreen Company | Garcoa, Inc. | SV Labs Toronto Corporation
Effective date
2024-10-30
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:17:44

Label at a glance#

ProductWalgreens Pain Relieving with Turmeric Analgesic
Active ingredientLIDOCAINE HYDROCHLORIDE
Label structure11 sections

Dosage and administration

Adults and children 12 years of age and older: Apply to affected area not more than 3 to 4 times daily. Children under 12 years of age, consult a doctor.

Storage and handling

store at room temperature.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Lidocaine HCl 4%

Purpose

OTC - PURPOSE SECTION

Topical analgesic

Use

INDICATIONS & USAGE SECTION

for the temporary relief of pain.

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

  • Use only as directed. Read and follow all directions and warnings on this carton
  • Do not apply over large areas of the body.
  • Do not use on cut, irritated or swollen skin. Do not use on puncture wounds.
  • Do not bandage or apply local heat (such as heating pads) to the area of use or use with a medicated patch.
  • Do not allow contact with eyes or mucous membranes.
  • Do not use at the same time as other topical analgesics.

Discontinue use and consult a doctor if

OTC - STOP USE SECTION

  • condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days
  • redness is present
  • irritation develops

Flammable

SPL UNCLASSIFIED SECTION

  • keep away from fire or flame

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years of age and older: Apply to affected area not more than 3 to 4 times daily. Children under 12 years of age, consult a doctor.

Other information

STORAGE AND HANDLING SECTION

store at room temperature.

Inactive ingredients

INACTIVE INGREDIENT SECTION

acrylates/C10-30 alkyl acrylate crosspolymer, alcohol denat., aloe barbadensis leaf juice, aminomethyl propanol, C30-45 alkyl cetearyl dimethicone crosspolymer, caprylyl methicone, cetearyl alcohol, ceteth-20 phosphate, curcuma longa (turmeric) root extract, dicetyl phosphate, dimethicone, disodium EDTA, ethylhexylglycerin, glycerin, glyceryl stearate, isohexadecane, leuconostoc/radish root ferment filtrate, phenoxyethanol, polysorbate 60, steareth-21, water.

Questions or comments?

OTC - QUESTIONS SECTION

1-800-925-4733

SPL UNCLASSIFIED SECTION

DISTRIBUTED BY: WALGREEN CO.
200 WILMONT RD., DEERFIELD, IL 60015

PRINCIPAL DISPLAY PANEL - 73 mL Bottle Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Walgreens

WALGREENS
•PHARMACIST RECOMMENDED†•

Pain Relieving
Liquid with
Turmeric

LIDOCAINE 4% / TOPICAL ANALGESIC

MAXIMUM STRENGTH LIDOCAINE

For temporary relief of pain

Easy to apply to affected area

No-mess applicator

Fragrance free

2.5 FL OZ (73 mL)

PRINCIPAL DISPLAY PANEL - 73 mL Bottle Carton
PRINCIPAL DISPLAY PANEL - 73 mL Bottle Carton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1987647lidocaine hydrochloride 4 % Topical SolutionPSN3
1987647lidocaine hydrochloride 40 MG/ML Topical SolutionSCD3
1987647lidocaine hydrochloride 4 % Topical SolutionSY3

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
LIDOCAINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
070fbed5-7088-434a-a7ce-f2a64d8d40acProduct name220260107
bee66ce1-adb7-9d3b-67d9-582e4c54e80fProduct name520250819
860a93dc-4863-49cc-b284-6bbe8191bc48Product name420250214
eaba870a-6a9d-442e-8643-87b3f558a451Product name120250117
9b4cf230-fd05-41d5-98c6-5db9ecb27b86Product name120230117
7d755fa1-1087-4dcd-98f0-6d4bba479a57Product name320210602
aed701d5-9c75-dfaf-7154-cde46179faeaProduct name920200313
fa8b5901-e681-426f-82fe-54f6d81ec698Product name420180619
332d03e4-aa24-4b11-841a-02bf41081920Product name120171221
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070Product name120171221
68ed98f8-24c2-44a0-944a-6d36e82ce25aProduct name120141222
1cd42bc2-a430-c72b-636d-991b235fbf80Product name120140508
49fa150c-f0de-cce7-3d9c-993ed81c5698Product name120140508
4d7ae718-ed00-bae8-2abe-9eaec1eef7ffProduct name120140508
9137811f-f279-8640-5aeb-99fa2145d64dProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-1222-01Walgreens Pain Relieving with TurmericAnalgesic73 mL in 1 BOTTLE, WITH APPLICATORLIQUID733
0363-1222-01Walgreens Pain Relieving with TurmericAnalgesic1 in 1 CARTONLIQUID13

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-12220363-1222-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 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
Walgreens Pain Relieving with Turmeric AnalgesicLIDOCAINE HYDROCHLORIDEWalgreen Company317ec4fb-cff0-461d-9ca0-299527a3686d2024-10-30WarningsExact identifier
ndc (package): 0363-1222-01
ndc (product): 0363-1222
ndc11 (package): 00363122201
spl id: 43585b52-5a9c-401c-81e5-a2082a328d94
spl set id: 317ec4fb-cff0-461d-9ca0-299527a3686d

Reported adverse events (FAERS/openFDA)#

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