Home NDC 29784-602 Profoot Plantar Relief Strips
Product NDC 29784-602
11-digit product format 297840602
Labeler code 29784
Product ID 29784-602_2529f702-e4dc-6c83-e063-6294a90ab89e
Type HUMAN OTC DRUG
Nonproprietary name CAMPHOR (NATURAL), MENTHOL, METHYL SALICYLATE
Dosage form PATCH
Route TOPICAL
Labeler Rooftop Consumer Health, Inc.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-10-18
Marketing end 2027-05-31
Substance CAMPHOR (NATURAL); MENTHOL; METHYL SALICYLATE
Active strength 12; 57; 63 mg/g; mg/g; mg/g
NDC exclude flag No
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 Profoot Plantar Relief Strips Active Ingredients# Ingredient, Strength table Ingredient Strength CAMPHOR (NATURAL) 12 mg/g MENTHOL 57 mg/g METHYL SALICYLATE 63 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination N20HL7Q941 Internal UNII lookup L7T10EIP3A Internal UNII lookup LAV5U5022Y Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 853260 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 29784-602-01 Profoot Plantar Relief Strips 4 in 1 POUCH PATCH 4 2 29784-602-01 Profoot Plantar Relief Strips 1 in 1 BOX PATCH 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 29784-602 PROFOOT PLANTAR RELIEF STRIPS (CAMPHOR (NATURAL), MENTHOL, METHYL SALICYLATE) PATCH [ROOFTOP CONSUMER HEALTH, INC.] 2 Current NDC, 2 package rows 20241025_65e142d8-da21-4c55-9faf-b387cb6c2c0e.zip
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 8 of 156 · 3,115 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 29784-602-01 29784060201 1 POUCH in 1 BOX (29784-602-01) / 4 PATCH in 1 POUCH / 1.03 g in 1 PATCH 1 pouch 2023-10-18 2027-05-31 No No Historical