Label: GURUNANDA PAIN RELIEF- menthol and camphor ointment
- NDC Code(s): 70708-937-13, 70708-937-18
- Packager: GURUNANDA, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 24, 2025
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- Uses
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Warnings
For external use only.
When using this product
use only as directed, avoid contact with eye and mucous membranes, do not apply to wounds, damaged or irritated skin, do not bandage or cover with wrap or heating pad, do not use 1 hour prior to bathing or within 30 minutes after bathing
Stop use and ask a doctor if
- condition worsens
- severe skin irritaiton occurs
- pain persists for more than 7 days
- pain clears up and then recurs a few days later
- Directions
- Other information
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
GURUNANDA PAIN RELIEF
menthol and camphor ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70708-937 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC) 110 mg in 1 g MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 110 mg in 1 g Inactive Ingredients Ingredient Name Strength PEPPERMINT OIL (UNII: AV092KU4JH) PARAFFIN (UNII: I9O0E3H2ZE) CHINESE CINNAMON OIL (UNII: A4WO0626T5) CLOVE OIL (UNII: 578389D6D0) CAJUPUT OIL (UNII: J3TO6BUQ37) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70708-937-13 1 in 1 CARTON 09/01/2025 1 14.2 g in 1 JAR; Type 0: Not a Combination Product 2 NDC:70708-937-18 1 in 1 CARTON 09/01/2025 2 18 g in 1 JAR; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 09/01/2025 Labeler - GURUNANDA, LLC (079671169)


