Home NDC 61734-301 La Vaquita
Product NDC 61734-301
11-digit product format 617340301
Labeler code 61734
Product ID 61734-301_5a6ebccd-9b61-12ef-e063-6394a90a4cf3
Type HUMAN OTC DRUG
Nonproprietary name Methyl Salicylate, Menthol
Dosage form OINTMENT
Route TOPICAL
Labeler Delon Laboratories (1990) Ltd
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2011-04-26
Substance METHYL SALICYLATE; MENTHOL
Active strength 12; 3 g/100g; g/100g
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 6 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…
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 La Vaquita
Brand name suffix New Extra
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength METHYL SALICYLATE 12 g/100g MENTHOL 3 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination LAV5U5022Y 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 1111032 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 61734-301-01 La VaquitaNew Extra 90 g in 1 CAN OINTMENT 90 16 61734-301-02 La VaquitaNew Extra 100 g in 1 JAR OINTMENT 100 16
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded MENTHOL ACTIVE INGREDIENT L7T10EIP3A LA VAQUITA NEW EXTRA (METHYL SALICYLATE, MENTHOL) OINTMENT [DELON LABORATORIES (1990) LTD] 3 Methyl Salicylate ACTIVE INGREDIENT LAV5U5022Y LA VAQUITA NEW EXTRA (METHYL SALICYLATE, MENTHOL) OINTMENT [DELON LABORATORIES (1990) LTD] 3 MENTHOL ACTIVE MOIETY L7T10EIP3A LA VAQUITA NEW EXTRA (METHYL SALICYLATE, MENTHOL) OINTMENT [DELON LABORATORIES (1990) LTD] 3 Methyl Salicylate ACTIVE MOIETY LAV5U5022Y LA VAQUITA NEW EXTRA (METHYL SALICYLATE, MENTHOL) OINTMENT [DELON LABORATORIES (1990) LTD] 3 D&C RED NO. 17 INACTIVE INGREDIENT ND733RX3JN LA VAQUITA NEW EXTRA (METHYL SALICYLATE, MENTHOL) OINTMENT [DELON LABORATORIES (1990) LTD] 3 LANOLIN INACTIVE INGREDIENT 7EV65EAW6H LA VAQUITA NEW EXTRA (METHYL SALICYLATE, MENTHOL) OINTMENT [DELON LABORATORIES (1990) LTD] 3 PARAFFIN INACTIVE INGREDIENT I9O0E3H2ZE LA VAQUITA NEW EXTRA (METHYL SALICYLATE, MENTHOL) OINTMENT [DELON LABORATORIES (1990) LTD] 3 PETROLATUM INACTIVE INGREDIENT 4T6H12BN9U LA VAQUITA NEW EXTRA (METHYL SALICYLATE, MENTHOL) OINTMENT [DELON LABORATORIES (1990) LTD] 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 61734-301 LA VAQUITA NEW EXTRA (METHYL SALICYLATE, MENTHOL) OINTMENT [DELON LABORATORIES (1990) LTD] 15 Current NDC, Legacy NDC, 2 package rows 20250212_3097a01b-cee5-492f-b65a-63992fb28e3a.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 149 of 151 · 3,020 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join SCLERA CARE Topical Anesthetic Gel LIDOCAINE HYDROCHLORIDE ScleraCare, LLC 488ace02-fc0b-4d13-ab89-0e1640e915e5 2023-11-05 Warnings Exact identifier application number: M017 IRELIEV ROLL ON COOL PAIN RELIEF MENTHOL Excel Health, Inc dab94995-7393-4d9c-b295-72611a90919b 2023-11-05 Warnings Exact identifier application number: M017 URIFLEX Fast Acting Analgesic Pain Relief MENTHOL Rejuvica LLC fb78f705-b838-461d-b42c-8c98d3ca5d09 2023-11-05 Warnings Exact identifier application number: M017 365 Medicated Lip Balm MEDICATED LIP BALM Whole Foods Market, Inc. 48309a7d-d2da-483c-8bf8-f59d9ad0bb73 2023-11-03 Warnings Exact identifier application number: M017 COOL BREEZE Pain Relief MENTHOL COOL BREEZE US LLC 14dcf4ee-6778-49d4-8601-9205737432ea 2023-11-01 Warnings Exact identifier application number: M017 Lidozen LIDOCAINE HYDROCHLORIDE, MENTHOL Proficient Rx LP 1ebb45e5-4541-4c95-abe1-661ef763a610 2023-11-01 Warnings Exact identifier application number: M017 Walgreens Pain Relieving Cream LIDOCAINE 4% Walgreens ce1b55ed-f5c5-ea8b-e053-2a95a90acd40 2023-10-31 Warnings Exact identifier application number: M017 Walgreens pain relieving LIDOCAINE 4% Walgreens ce2b9e57-749d-715c-e053-2995a90aaf8d 2023-10-31 Warnings Exact identifier application number: M017 Walgreens Cool n heat LIDOCAINE 4% MENTHOL 1% Walgreens ce168ab7-ec4a-daea-e053-2995a90af829 2023-10-31 Warnings Exact identifier application number: M017 Methyl Salicylate 40 Percent METHYL SALICYLATE Alexso, Inc 53407aab-094c-4393-a2b9-54fd85321e3e 2023-10-31 Warnings Exact identifier application number: M017 Hydrocortisone Acetate HYDROCORTISONE ACETATE Bentlin Products LLC 4346351c-8e11-46ae-b428-98d17f55beb9 2023-10-30 Warnings Exact identifier application number: M017 Biofreeze Roll-On MENTHOL A-S Medication Solutions 814b37ea-5441-4cec-8794-71ca01d849ae 2023-10-30 Warnings Exact identifier application number: M017 Dr. Sheffield Hydrocortisone Anti itch HYDROCORTISONE Sheffield Pharmaceuticals LLC 71c9f2f4-2188-45eb-b55e-3856ac78070b 2023-10-30 Warnings Exact identifier application number: M017 Family Wellness BENZOCAINE, RESORCINOL Zhejiang Jingwei Pharmaceutic Al Co., Ltd. df540eb8-6773-4647-9cc2-c3fd14d7355e 2023-10-27 Warnings Exact identifier application number: M017 Family Wellness HYDROCORTISONE 1% FRONT PHARMACEUTICAL PLC ea26265d-f24e-458e-8bf0-287b2d49f4f4 2023-10-27 Warnings Exact identifier application number: M017 Joint Formula 88 MAX PLUS CAMPHOR Sarati International, Inc. f5d78335-b78d-4909-a88b-9daa3c18ba15 2023-10-27 Warnings Exact identifier application number: M017 OsmoFlex MENTHOL Sarati International, Inc. 479147c0-4cf4-4d7a-8b8e-1a0de49ed73e 2023-10-27 Warnings Exact identifier application number: M017 Thera plus Anti-itch with aloe Hydrocortisone HYDROCORTISONE Fourstar Group USA, Inc. c69d0670-a65b-1680-e053-2995a90a2ee5 2023-10-26 Warnings Exact identifier application number: M017 Family Wellness DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE FRONT PHARMACEUTICAL PLC fde2069b-344e-46da-bb95-c5113e0f35d6 2023-10-26 Warnings Exact identifier application number: M017 MAXIMUM STRENGTH HEMORRHOIDAL RELIEF LIDOCAINE CVS PHARMACY, INC b61424bf-3b23-420b-a7bc-256ddb96aa22 2023-10-25 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 61734-301-01 61734030101 90 g in 1 CAN (61734-301-01) 90 g 2014-10-04 0000-00-00 No No Current 61734-301-02 61734030102 100 g in 1 JAR (61734-301-02) 100 g 2018-07-18 0000-00-00 No No Current