Home NDC 70708-834 GuruNanda Pain Relief
Product NDC 70708-834
11-digit product format 707080834
Labeler code 70708
Product ID 70708-834_48c6c231-7293-18b6-e063-6294a90aa02e
Type HUMAN OTC DRUG
Nonproprietary name Menthol
Dosage form SPRAY
Route TOPICAL
Labeler GURUNANDA, LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-09-01
Substance LEVOMENTHOL
Active strength 105 mg/mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base GuruNanda Pain Relief
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LEVOMENTHOL 105 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination BZ1R15MTK7 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1489073 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70708-834-02 GuruNanda Pain Relief 59 mL in 1 BOTTLE, SPRAY SPRAY 59 3 70708-834-02 GuruNanda Pain Relief 1 in 1 CARTON SPRAY 1 3
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 116 of 152 · 3,029 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 70708-834-02 70708083402 1 BOTTLE, SPRAY in 1 CARTON (70708-834-02) / 59 mL in 1 BOTTLE, SPRAY 2025-09-01 No No Current