Home NDC 70673-297 SMOOTH GATOR Foot and Leg Rub
Product NDC 70673-297
11-digit product format 706730297
Labeler code 70673
Product ID 70673-297_09d7554e-93a1-9886-e063-6394a90a1a85
Type HUMAN OTC DRUG
Nonproprietary name CAMPHOR (SYNTHETIC), MENTHOL
Dosage form CREAM
Route TOPICAL
Labeler Smooth Gator LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-06-01
Substance CAMPHOR (SYNTHETIC); MENTHOL
Active strength 40; 12.5 mg/g; mg/g
NDC exclude flag No
Listing certified through 2026-12-31
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 SMOOTH GATOR Foot and Leg Rub
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength CAMPHOR (SYNTHETIC) 40 mg/g MENTHOL 12.5 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 5TJD82A1ET Internal UNII lookup L7T10EIP3A Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2604039 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 70673-297-08 SMOOTH GATOR Foot and Leg Rub 227 g in 1 BOTTLE CREAM 227 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70673-297 SMOOTH GATOR FOOT AND LEG RUB (CAMPHOR (SYNTHETIC), MENTHOL) CREAM [SMOOTH GATOR LLC] 2 Current NDC, Legacy NDC, 1 package rows 20231111_57094238-506b-48c1-8eb9-fe904be80df0.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 111 of 151 · 3,020 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join HealthWise Medicated Original Body Powder 10 oz MENTHOL Veridian Healthcare 296b623a-14cd-0bca-e063-6394a90ac5ff 2024-12-16 Warnings Exact identifier application number: M017 HealthWise Medicated Extra Body Powder 10 oz MENTHOL Veridian Healthcare 296c9a9c-e3db-59fe-e063-6294a90a0b62 2024-12-16 Warnings Exact identifier application number: M017 Rite Aid Hot and Cold Roll On MENTHOL 16% Rite Aid fc4b2635-280b-267f-e053-6294a90a5e22 2024-12-15 Warnings Exact identifier application number: M017 Rite Aid Pain Relieving BENZOCAINE 20%, MENTHOL 0.5% Rite Aid e2c09e85-be0a-4e6d-e053-2995a90ad756 2024-12-15 Warnings Exact identifier application number: M017 Rugby Lidocaine LIDOCAINE 4% Rugby Laboratories d94292f7-10fc-48bf-e053-2995a90a8472 2024-12-15 Warnings Exact identifier application number: M017 Rite Aid Cortisone HYDROCORTISONE 1% Rite Aid e27353b9-23b6-3801-e053-2a95a90a6045 2024-12-15 Warnings Exact identifier application number: M017 Rite Aid Cooling Pain Relief MENTHOL 10.5% Rite Aid e2225259-70ec-52de-e053-2a95a90a73f8 2024-12-15 Warnings Exact identifier application number: M017 Rite Aid Rectal Care LIDOCAINE 5% Rite Aid e283e462-96e8-04cf-e053-2a95a90a1d00 2024-12-15 Warnings Exact identifier application number: M017 Rite Aid Anti-Itch DIPHENHYDRAMINE HCL 2% Rite Aid e33898d8-1b8b-5c0b-e053-2995a90add08 2024-12-15 Warnings Exact identifier application number: M017 Rite Aid Cala Itch Relief PRAMOXINE HCL 1%, ZINC ACETATE 0.1% Rite Aid e29a9d59-4c7c-81aa-e053-2995a90a7056 2024-12-15 Warnings Exact identifier application number: M017 CVS Roll-On CAPSAISIN 0.1% CVS e8812c49-335e-61ea-e053-2995a90a17aa 2024-12-15 Warnings Exact identifier application number: M017 Good Sense Burn Relief Aloe LIDOCAINE HCL Geiss, Destin & Dunn, Inc b5a7f629-a88d-b49d-e053-2995a90a49fa 2024-12-15 Warnings Exact identifier application number: M017 QC Burn Relief Aloe LIDOCAINE HCL Chain Drug Marketing Association Inc b5e76f0c-0bfe-b13e-e053-2995a90a0861 2024-12-15 Warnings Exact identifier application number: M017 Meijer Burn Relief LIDOCAINE 0.5% Meijer bec60c93-5abd-ee04-e053-2a95a90acb61 2024-12-15 Warnings Exact identifier application number: M017 QC Cool and Heat Roll-On MENTHOL 16% Chain Drug Marketing Association Inc d35e9dfa-8a28-fdb3-e053-2995a90abc52 2024-12-15 Warnings Exact identifier application number: M017 Meijer Cold and Hot Pain Relieving MENTHOL 16% Meijer bec62df3-06c9-a115-e053-2995a90a4267 2024-12-15 Warnings Exact identifier application number: M017 Tommie Copper Pain Relief MENTHOL 16% Tommie Copper, Inc. b4dfa5fa-2d61-db1e-e053-2a95a90a7ac8 2024-12-15 Warnings Exact identifier application number: M017 Pain Relief Liquid Roller CAMPHOR 3.5%, MENTHOL 3.5% Tommie Copper, Inc. c9f0447e-de43-16a5-e053-2995a90a05c1 2024-12-15 Warnings Exact identifier application number: M017 Tommie Copper Pain Relief Maximum Strength TROLAMINE SALICYLATE 10% Tommie Copper, Inc. b622c14f-9bf3-0bbd-e053-2a95a90a2adc 2024-12-15 Warnings Exact identifier application number: M017 Copperlife Pain Relief TROLAMINE SALICYLATE 10% Tommie Copper, Inc. c94d00f9-42ce-1d43-e053-2a95a90a058d 2024-12-15 Warnings Exact identifier application number: M017
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 70673-297-08 70673029708 227 g in 1 BOTTLE (70673-297-08) 227 g 2022-06-01 0000-00-00 No No Current