GuruNanda Lidocaine 4% Rain Relief Spray with Mangnesium

Manufacturer
GuruNanda, LLC.
Effective date
2025-11-10
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:43:06

Label at a glance#

ProductGuruNanda Pain Relief
Active ingredientLIDOCAINE HYDROCHLORIDE
Label structure8 sections

Indications and uses

for temporary relief of pain

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: Do not use. Consult a doctor

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Lidocaine HCI 4%

OTC - PURPOSE SECTION

Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

for temporary relief of pain

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

  • in large quantities, particularly over raw surfaces or blistered areas
  • on wounds or damaged skin
  • with a heating pad
  • if you are allergic to any ingredients of this product

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

sensitive skin or kidney problems

When using this product

OTC - WHEN USING SECTION

  • use only as directed. Read and follow all directions and warnings on this label
  • avoid contact with eyes and mucous membranes
  • do not apply to irritated skin or if excessive irriation develops
  • avoid spraying on face
  • avoid inhalation of spray
  • avoid applying to skin folds
  • do not bandage or apply local heat (such as heating pads) or a medicated patch to area of use
  • do not use at the same time as other topical analgesic

Stop use and ask a doctor if

OTC - STOP USE SECTION

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

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

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 immediately (1-800-222-1222)

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: Do not use. Consult a doctor

Other information

OTHER SAFETY INFORMATION

  • Do not use if printed seal is broken or missing
  • Store the product in a cool, dry place, away from direct sunlight and excessive moisture

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Magnesium Chloride, PEG-40 Hydrogenated Castor Oil, Benzyl Alcohol, Arnica Montana Flower Extract, Ginger Oil, Peppermint Oil, Cholecalciferol (Vitamin D3), Wintergreen Oil, D-Alpha Tocopherol (Vitamin E), Black Pepper Oil, Menaquinone-7 (Vitamin K2), Caprylic/Capric/Lauric Triglyceride

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

088353088353

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1045432lidocaine HCl 4 % Topical SprayPSN3
1045432lidocaine hydrochloride 40 MG/ML Topical SpraySCD3
1045432lidocaine HCl 4 % Topical SpraySY3
1045432lidocaine HCl 4 % Topical Spray GelSY3

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
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
9b4cf230-fd05-41d5-98c6-5db9ecb27b86Product name120230117
7d755fa1-1087-4dcd-98f0-6d4bba479a57Product name320210602
aed701d5-9c75-dfaf-7154-cde46179faeaProduct name920200313
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
fa8b5901-e681-426f-82fe-54f6d81ec698Product name420180619
332d03e4-aa24-4b11-841a-02bf41081920Product name120171221
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070Product name120171221
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
68ed98f8-24c2-44a0-944a-6d36e82ce25aProduct name120141222
1cd42bc2-a430-c72b-636d-991b235fbf80Product name120140508
49fa150c-f0de-cce7-3d9c-993ed81c5698Product name120140508
4d7ae718-ed00-bae8-2abe-9eaec1eef7ffProduct name120140508
60c52429-fcef-eb54-2387-43bc9e4f296bProduct name120140508
9137811f-f279-8640-5aeb-99fa2145d64dProduct name120140508
9869efd7-d6dd-0665-5b67-53adbe6ef15eProduct name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70708-101-02GuruNanda Pain Relief59 mL in 1 BOTTLE, SPRAYSPRAY593
70708-101-02GuruNanda Pain Relief1 in 1 CARTONSPRAY13

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70708-10170708-101-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22025-07-25full-release2026-06-01 01:10:32

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
GuruNanda Pain ReliefLIDOCAINE HYDROCHLORIDEGuruNanda, LLC.3ab6a133-8dca-e14e-e063-6394a90a85e72025-11-10WarningsExact identifier
ndc (package): 70708-101-02
ndc (product): 70708-101
ndc11 (package): 70708010102
spl id: 4346e8ec-7cdf-56f3-e063-6294a90af0a2
spl set id: 3ab6a133-8dca-e14e-e063-6394a90a85e7

Reported adverse events (FAERS/openFDA)#

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