Home NDC 43136-593 HIMALAYA PINK SALT Purple Color Corrector plus Intensive Whitening Vanilla Mint
Product NDC 43136-593
11-digit product format 431360593
Labeler code 43136
Product ID 43136-593_2698d6ea-3e60-5d60-e063-6394a90aaa69
Type HUMAN OTC DRUG
Nonproprietary name Sodium Fluoride
Dosage form PASTE, DENTIFRICE
Route DENTAL
Labeler Tai Guk Pharma. Co., Ltd.
Application M021
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-11-01
Substance SODIUM FLUORIDE
Active strength 1.5 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 HIMALAYA PINK SALT Purple Color Corrector plus Intensive Whitening Vanilla Mint
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SODIUM FLUORIDE 1.5 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 8ZYQ1474W7 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 891775 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 43136-593-11 HIMALAYA PINK SALT Purple Color Corrector plus Intensive Whitening Vanilla Mint 1 in 1 CARTON PASTE, DENTIFRICE 1 1 43136-593-11 HIMALAYA PINK SALT Purple Color Corrector plus Intensive Whitening Vanilla Mint 100 g in 1 TUBE PASTE, DENTIFRICE 100 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 43136-593 HIMALAYA PINK SALT PURPLE COLOR CORRECTOR PLUS INTENSIVE WHITENING VANILLA MINT (SODIUM FLUORIDE) PASTE, DENTIFRICE [TAI GUK PHARMA. CO., LTD.] 1 Current NDC, 2 package rows 20241112_2698d6d8-051b-6c10-e063-6394a90a9418.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 45 of 50 · 995 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 43136-593-11 43136059311 1 TUBE in 1 CARTON (43136-593-11) / 100 g in 1 TUBE 1 tube 2024-11-01 No No Current