Home NDC 11673-832 Children Allergy Relief
Product NDC 11673-832
11-digit product format 116730832
Labeler code 11673
Product ID 11673-832_919914be-4102-46a6-bbf6-f82ac464799c
Type HUMAN OTC DRUG
Nonproprietary name Diphenhydramine HCl
Dosage form LIQUID
Route ORAL
Labeler TARGET CORPORATION
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-04-17
Substance DIPHENHYDRAMINE HYDROCHLORIDE
Active strength 12.5 mg/5mL
Pharmacologic classes Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
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 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2024-03-11 06:39 UTC · source 2024-03-08 excluded product product 11673-832 I Inactivated by FDA excluded / ndc_excluded.zip 1332a3947898…d4bfe170f9cd…2024-03-11 06:39 UTC · source 2024-03-08 excluded package package 11673-832 11673-832-04 I Inactivated by FDA excluded / ndc_excluded.zip 1332a3947898…d4bfe170f9cd…
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 Children Allergy Relief
Brand name suffix Bubblegum flavor
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DIPHENHYDRAMINE HYDROCHLORIDE 12.5 mg/5mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination TC2D6JAD40 Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 11673-832-04 Children Allergy ReliefBubblegum flavor 118 mL in 1 BOTTLE, PLASTIC LIQUID 118 5 11673-832-04 Children Allergy ReliefBubblegum flavor 1 in 1 CARTON LIQUID 1 5 11673-832-08 Children Allergy ReliefBubblegum flavor 118 mL in 1 BOTTLE, PLASTIC LIQUID 118 5 11673-832-08 Children Allergy ReliefBubblegum flavor 2 in 1 CARTON LIQUID 2 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 11673-832 CHILDREN ALLERGY RELIEF BUBBLEGUM FLAVOR (DIPHENHYDRAMINE HCL) LIQUID [TARGET CORPORATION] 4 Current NDC, Legacy NDC, 4 package rows 20241109_69d33f77-06e1-48fa-a516-892fdf11bb1c.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 174 of 174 · 3,464 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join DEXTROMETHORPHAN HYDROBROMIDE, Guaifenesin, and PHENYLEPHRINE HYDROCHLORIDE DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, AND PHENYLEPHRINE HYDROCHLORIDE Westminster Pharmaceuticals, LLC a58bfb14-28f9-4425-a5a5-aaff4847c979 2018-03-14 Warnings Exact identifier application number: M012 Chlorpheniramine maleate 4mg CHLORPHENIRAMINE MALEATE 4MG Athlete's Needs, Inc. 4d974959-25fc-4707-9b72-9afbf47b76f1 2017-11-14 Warnings Exact identifier application number: M012 Cold Medicine ACETAMINOPHEN, CHLORPHENIRAMINE MALEATE, PHENYLEPHRINE HCL Selder, S.A. de C.V. d2762d9c-e7e7-42b2-a26a-14b2aa0307cb 2017-01-25 Warnings Exact identifier application number: M012 Allergy CHLORPHENIRAMINE MALEATE Marc Glassman, Inc. 2051247f-ce64-4cf5-b449-9ca14c43ab86 2016-12-27 Warnings Exact identifier application number: M012
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 11673-832-04 11673083204 1 BOTTLE, PLASTIC in 1 CARTON (11673-832-04) / 118 mL in 1 BOTTLE, PLASTIC 2019-04-17 0000-00-00 No No Current 11673-832-08 11673083208 2 BOTTLE, PLASTIC in 1 CARTON (11673-832-08) / 118 mL in 1 BOTTLE, PLASTIC 2025-05-15 No No Current