FDA.reportPublic FDA data

GuruNanda Pain Relief Spray

Manufacturer
GURUNANDA, LLC
Effective date
2026-01-19
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 01:33:52

Label at a glance#

ProductGuruNanda Pain Relief
Active ingredientLEVOMENTHOL
Label structure8 sections

Dosage and administration

Adults and children 12 years of age and older: Spray affected area not more than 3 to 4 times daily Children under 12 years of age: Ask a health professional before use. Children under 2 years of age: Do not use

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 10.5%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Use

INDICATIONS & USAGE SECTION

temporariliy relieves minor aches and pains of muscles and joints

Warnings

WARNINGS SECTION

For external use only

Flammable Do not use near heat, fire, flame, sparks or while smoking

Do not use

OTC - DO NOT USE SECTION

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

Stop use and ask a doctor if

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 days, you experience signs of skin injury, such as pain, swelling, or blistering where the product was applied.

When using this product

OTC - WHEN USING SECTION

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

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: Spray affected area not more than 3 to 4 times daily

Children under 12 years of age: Ask a health professional before use.

Children under 2 years of age: Do not use

Other information

OTHER SAFETY INFORMATION

  • Recommended storage temperature 59°F-77°F (15°C-25°C)
  • Do not store at temperature above 120°F (49°C)
  • Do not use if printed neck seal is broken or missing

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

08834.108834.1

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1489073menthol 10.5 % Topical SprayPSN3
1489073menthol 105 MG/ML Topical SpraySCD3
1489073menthol 10.5 % Topical SpraySY3

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
60c52429-fcef-eb54-2387-43bc9e4f296bProduct name120140508
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70708-834-02GuruNanda Pain Relief59 mL in 1 BOTTLE, SPRAYSPRAY593
70708-834-02GuruNanda Pain Relief1 in 1 CARTONSPRAY13

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70708-83470708-834-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
.ALPHA.-TOCOPHEROL, D-N9PR3490H9IACT
ARNICA MONTANA FLOWEROZ0E5Y15PZIACT
LEVOMENTHOLBZ1R15MTK7ACTIB
EUCALYPTUS OIL2R04ONI662IACT
PEPPERMINT OILAV092KU4JHIACT
CHOLECALCIFEROL1C6V77QF41IACT
ALCOHOL3K9958V90MIACT
GINGER OILSAS9Z1SVUKIACT
WATER059QF0KO0RIACT
BLACK PEPPER OILU17J84S19ZIACT
LAVENDER OILZBP1YXW0H8IACT
MAGNESIUM CHLORIDE02F3473H9OIACT
MENAQUINONE-78427BML8NYIACT
CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDEFJ1H6M2JG9IACT
FRANKINCENSE OIL67ZYA5T02KIACT
GAULTHERIA PROCUMBENS (WINTERGREEN) LEAF OILLAV5U5022YIACT

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
GuruNanda Pain ReliefMENTHOLGURUNANDA, LLC3f1d146e-0d18-7f2f-e063-6394a90ab8162026-01-19WarningsExact identifier
ndc (package): 70708-834-02
ndc (product): 70708-834
ndc11 (package): 70708083402
spl id: 48c6c231-7293-18b6-e063-6294a90aa02e
spl set id: 3f1d146e-0d18-7f2f-e063-6394a90ab816

Reported adverse events (FAERS/openFDA)#

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