Home NDC 87957-004 TideFresh SMELLING SALTS
Product NDC 87957-004
11-digit product format 879570004
Labeler code 87957
Product ID 87957-004_5a27a35c-8c6c-d298-e063-6294a90a1389
Type HUMAN OTC DRUG
Nonproprietary name Menthol 15% SMELLING SALTS
Dosage form INHALANT
Route RESPIRATORY (INHALATION)
Labeler Hubei Minxin Pharmaceutical Co., Ltd.
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2026-08-29
Substance MENTHOL
Active strength 15 g/100g
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 TideFresh SMELLING SALTS
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL 15 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 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 2749971 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 87957-004-01 87957000401 40 g in 1 BOTTLE (87957-004-01) 40 g 2026-08-29 No No Current