Home NDC 43136-105 AVON HeXashield Congestion Relief
Product NDC 43136-105
11-digit product format 431360105
Labeler code 43136
Product ID 43136-105_2aabc954-bc58-e806-e063-6394a90a05dd
Type HUMAN OTC DRUG
Nonproprietary name OXYMETAZOLINE HYDROCHLORIDE
Dosage form SPRAY
Route NASAL
Labeler Tai Guk Pharm. Co., Ltd.
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-07-31
Substance OXYMETAZOLINE HYDROCHLORIDE
Active strength .05 g/mL
Pharmacologic classes Imidazolines [CS], Increased Sympathetic Activity [PE], Vasoconstriction [PE], Vasoconstrictor [EPC]
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 AVON HeXashield Congestion Relief
Brand name suffix Original
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength OXYMETAZOLINE HYDROCHLORIDE .05 g/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination K89MJ0S5VY Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1000990 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 43136-105-01 AVON HeXashield Congestion ReliefOriginal 15 mL in 1 BOTTLE, SPRAY SPRAY 15 2 43136-105-01 AVON HeXashield Congestion ReliefOriginal 1 in 1 CARTON SPRAY 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 43136-105 AVON HEXASHIELD CONGESTION RELIEF ORIGINAL (OXYMETAZOLINE HYDROCHLORIDE) SPRAY [TAI GUK PHARM. CO., LTD.] 2 Current NDC, Legacy NDC, 2 package rows 20250103_8f2c152c-c564-0cba-e053-2a95a90ab3c7.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 74 of 180 · 3,583 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 43136-105-01 43136010501 1 BOTTLE, SPRAY in 1 CARTON (43136-105-01) / 15 mL in 1 BOTTLE, SPRAY 2019-07-31 0000-00-00 No No Current