NDC 31722-339-01 - Naproxen delayed release

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 31722-339
Requested NDC: 31722-339-01
Package NDCs from labels: 31722-339-01, 31722-339-05, 31722-339-10, 31722-339-50
Manufacturer: Preferred Pharmaceuticals Inc.
Effective date: 2019-11-01
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Naproxen Delayed-release Tablets USP, 375 mg and 500 mg	Preferred Pharmaceuticals Inc.	2019-11-01	HUMAN PRESCRIPTION DRUG LABEL
Naproxen Delayed-release Tablets USP, 375 mg and 500 mg	Blenheim Pharmacal, Inc.	2015-06-05	HUMAN PRESCRIPTION DRUG LABEL
Naproxen Delayed Release - Northwind Pharmaceuticals	Northwind Pharmaceuticals	2014-06-03	HUMAN PRESCRIPTION DRUG LABEL
Naproxen delayed release - Camber Pharmaceuticals \| Invagen Pharmaceuticals	Camber Pharmaceuticals \| Invagen Pharmaceuticals	2012-02-01	HUMAN PRESCRIPTION DRUG LABEL
National Council for Prescription Drug Programs indexing - billing unit	National Council for Prescription Drug Programs	2012-07-24	Indexing - Billing Unit

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
31722-339-05	2019-11-13	C162847	48780-1	97449f38-d247-f6ea-e053-dbdaa90aa703	Naproxen Delayed-release Tablets USP, 375 mg and 500 mg
31722-339-50	2019-11-13	C162847	48780-1	97449f38-d247-f6ea-e053-dbdaa90aa703	Naproxen Delayed-release Tablets USP, 375 mg and 500 mg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
31722-339-01	Naproxendelayed release	100 in 1 BOTTLE	TABLET	100	1
31722-339-05	Naproxendelayed release	24 in 1 CASE	TABLET	24	1
31722-339-10	Naproxendelayed release	500 in 1 BOTTLE	TABLET	500	1
31722-339-50	Naproxendelayed release	12 in 1 CASE	TABLET	12	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
31722-339	NAPROXEN DELAYED RELEASE (NAPROXEN) TABLET [CAMBER PHARMACEUTICALS]	1	Legacy NDC, 4 package rows	20120202_cb3897b7-d4f1-4081-bb3c-e5e270a84930.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
31722-339-01	EA - Each	31722-339	32fab88b-2546-4fb0-affb-67cc227e4c50	1	2012-07-24
31722-339-05	EA - Each	31722-339	f7adaa65-e901-4a7f-8479-75366991f577	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
NAPROXEN	ACTIVE INGREDIENT	57Y76R9ATQ	NAPROXEN DELAYED RELEASE (NAPROXEN) TABLET [BLENHEIM PHARMACAL, INC.]	2
NAPROXEN	ACTIVE MOIETY	57Y76R9ATQ	NAPROXEN DELAYED RELEASE (NAPROXEN) TABLET [BLENHEIM PHARMACAL, INC.]	2
CROSCARMELLOSE SODIUM	INACTIVE INGREDIENT	M28OL1HH48	NAPROXEN DELAYED RELEASE (NAPROXEN) TABLET [BLENHEIM PHARMACAL, INC.]	2
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	NAPROXEN DELAYED RELEASE (NAPROXEN) TABLET [BLENHEIM PHARMACAL, INC.]	2
METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A	INACTIVE INGREDIENT	NX76LV5T8J	NAPROXEN DELAYED RELEASE (NAPROXEN) TABLET [BLENHEIM PHARMACAL, INC.]	2
POVIDONE	INACTIVE INGREDIENT	FZ989GH94E	NAPROXEN DELAYED RELEASE (NAPROXEN) TABLET [BLENHEIM PHARMACAL, INC.]	2
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	NAPROXEN DELAYED RELEASE (NAPROXEN) TABLET [BLENHEIM PHARMACAL, INC.]	2
TALC	INACTIVE INGREDIENT	7SEV7J4R1U	NAPROXEN DELAYED RELEASE (NAPROXEN) TABLET [BLENHEIM PHARMACAL, INC.]	2
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	NAPROXEN DELAYED RELEASE (NAPROXEN) TABLET [BLENHEIM PHARMACAL, INC.]	2
TRIETHYL CITRATE	INACTIVE INGREDIENT	8Z96QXD6UM	NAPROXEN DELAYED RELEASE (NAPROXEN) TABLET [BLENHEIM PHARMACAL, INC.]	2
WATER	INACTIVE INGREDIENT	059QF0KO0R	NAPROXEN DELAYED RELEASE (NAPROXEN) TABLET [BLENHEIM PHARMACAL, INC.]	2
NAPROXEN	ACTIVE INGREDIENT	57Y76R9ATQ	NAPROXEN DELAYED RELEASE TABLET, DELAYED RELEASE [NORTHWIND PHARMACEUTICALS]	1
NAPROXEN	ACTIVE INGREDIENT	57Y76R9ATQ	NAPROXEN DELAYED RELEASE (NAPROXEN) TABLET [CAMBER PHARMACEUTICALS]	1
NAPROXEN	ACTIVE MOIETY	57Y76R9ATQ	NAPROXEN DELAYED RELEASE (NAPROXEN) TABLET [CAMBER PHARMACEUTICALS]	1
NAPROXEN	ACTIVE MOIETY	57Y76R9ATQ	NAPROXEN DELAYED RELEASE TABLET, DELAYED RELEASE [NORTHWIND PHARMACEUTICALS]	1
CROSCARMELLOSE SODIUM	INACTIVE INGREDIENT	M28OL1HH48	NAPROXEN DELAYED RELEASE (NAPROXEN) TABLET [CAMBER PHARMACEUTICALS]	1
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	NAPROXEN DELAYED RELEASE (NAPROXEN) TABLET [CAMBER PHARMACEUTICALS]	1
METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A	INACTIVE INGREDIENT	NX76LV5T8J	NAPROXEN DELAYED RELEASE (NAPROXEN) TABLET [CAMBER PHARMACEUTICALS]	1
POVIDONE	INACTIVE INGREDIENT	FZ989GH94E	NAPROXEN DELAYED RELEASE (NAPROXEN) TABLET [CAMBER PHARMACEUTICALS]	1
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	NAPROXEN DELAYED RELEASE (NAPROXEN) TABLET [CAMBER PHARMACEUTICALS]	1
TALC	INACTIVE INGREDIENT	7SEV7J4R1U	NAPROXEN DELAYED RELEASE (NAPROXEN) TABLET [CAMBER PHARMACEUTICALS]	1
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	NAPROXEN DELAYED RELEASE (NAPROXEN) TABLET [CAMBER PHARMACEUTICALS]	1
TRIETHYL CITRATE	INACTIVE INGREDIENT	8Z96QXD6UM	NAPROXEN DELAYED RELEASE (NAPROXEN) TABLET [CAMBER PHARMACEUTICALS]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	NAPROXEN DELAYED RELEASE (NAPROXEN) TABLET [CAMBER PHARMACEUTICALS]	1

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 7 of 149 · 2,967 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Rohto Sun and Sport	HYPROMELLOSE, POVIDONE	The Mentholatum Company	8bcc8882-b886-4b55-9bc4-d4b92a41358f	2026-06-19	Warnings	Exact identifier unii: FZ989GH94E
Rohto Dual Light Relief	HYPROMELLOSE, POVIDONE	The Mentholatum Company	1b597f83-d7f1-cf93-e063-6394a90a99f7	2026-06-19	Warnings	Exact identifier unii: FZ989GH94E
Creamy Beige Perfecting Makeup Broad Spectrum SPF 25	OCTINOXATE, TITANIUM DIOXIDE	Merle Norman Cosmetics, Inc	548b7c90-ef97-38ab-e063-6394a90ac609	2026-06-18	Warnings	Exact identifier unii: 15FIX9V2JP
Humalog	INSULIN LISPRO	Eli Lilly and Company	c8ecbd7a-0e22-4fc7-a503-faa58c1b6f3f	2026-06-16	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R
Naproxen	NAPROXEN	Coupler LLC	545fe39a-4777-b149-e063-6394a90a53cf	2026-06-16	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: 57Y76R9ATQ
GlowBiotics Tinted Sunscreen SPF 30	ZINC OXIDE	Rum Brands, LLC	544dba29-4785-4ab6-e063-6394a90a17b3	2026-06-16	Warnings	Exact identifier unii: 15FIX9V2JP
Societe Prime and Defend	ZINC OXIDE SUNSCREEN	Societe Clinical Skincare	5439bd31-5ee1-9bca-e063-6394a90a748c	2026-06-16	Warnings	Exact identifier unii: 15FIX9V2JP
Societe CoverShield Tinted SPF	ZINC OXIDE	Societe Clinical Skincare	545efbc4-82d4-f126-e063-6294a90a9710	2026-06-16	Warnings	Exact identifier unii: 15FIX9V2JP
H-Scars Formula	CALENDULA OFFICINALLIS, SILICEA	Healing Natural Oils LLC	8433ff00-d815-45e0-b0ec-1448668dd8f8	2026-06-16	Warnings	Exact identifier unii: ETJ7Z6XBU4
E-Z-GAS II	ANTACID/ANTIFLATULENT	E-Z-EM, INC.	4e12e1cb-b033-076d-e054-00144ff8d46c	2026-06-15	Warnings	Exact identifier unii: ETJ7Z6XBU4
Shield by HEALTHY SKIN LAB MD SUNSCREEN	TITANIUM DIOXIDE, ZINC OXIDE	HEALTHY SKIN LAB LIMITED	6838b754-9915-48ff-af35-5338dbd06ac4	2026-06-15	Warnings	Exact identifier unii: 15FIX9V2JP
BM BIO28 ALCOHOL	CALC SULPH, CALC FLUOR, CALC PHOS, FERR PHOS, KALI MUR, KALI PHOS, KALI SULPH, MAG PHOS, NAT PHOS, NAT SULPH, NAT MUR, SILICEA	Total Operations Management LLC DBA:Bestmade Natural Products Micro	544b66c4-49df-556f-e063-6394a90af3ed	2026-06-15	Warnings	Exact identifier unii: ETJ7Z6XBU4
SFL SUNSCREEN - SOL DEFENSE SPF 30	TITANIUM DIOXIDE, ZINC OXIDE	Lifeline Medical, Inc	5438c185-31c9-c51e-e063-6394a90ae9ef	2026-06-14	Warnings	Exact identifier unii: 15FIX9V2JP
BM Tooth Remineralization	CALC PHOS, CALC FLUOR, SILICEA	Total Operations Management LLC DBA:Bestmade Natural Products Micro	543bc298-ec32-38e9-e063-6394a90aac15	2026-06-14	Warnings	Exact identifier unii: ETJ7Z6XBU4
Nail Fungus Control Extra Strength	CALENDULA OFFICINALIS FLOWERING TOP, SILICON DIOXIDE, AND HYPERICUM PERFORATUM	Forces of Nature	d02b88a6-1999-4dcd-91b5-fad88a664fcb	2026-06-14	Warnings	Exact identifier unii: ETJ7Z6XBU4
Nerve Pain	ARABICA COFFEE BEAN, SILICON DIOXIDE, AND HYPERICUM PERFORATUM	Forces of Nature	a9c3ba2e-9254-4ccd-9fe9-7a360fdf2bb7	2026-06-14	Warnings	Exact identifier unii: ETJ7Z6XBU4
Scar Control	CALENDULA OFFICINALIS FLOWERING TOP, ALLYLTHIOUREA, AND SILICON DIOXIDE	Forces of Nature	595c3423-6b52-48fc-8a95-00b53c1ecc7b	2026-06-14	Warnings	Exact identifier unii: ETJ7Z6XBU4
BM BM186 DROPS	ARNICA, FERR PHOS, HYPERICUM, IGNATIA, SILICA	Total Operations Management LLC DBA:Bestmade Natural Products Micro	54243745-bd67-19c1-e063-6394a90a4b72	2026-06-13	Warnings	Exact identifier unii: ETJ7Z6XBU4
BM BM186 DROPS	ARNICA, FERR PHOS, HYPERICUM, IGNATIA, SILICA	BM Private Limited	540d8fbe-3bdb-1b54-e063-6394a90a114d	2026-06-12	Warnings	Exact identifier unii: ETJ7Z6XBU4
BM BM5 DROPS	APIS MELL, BAPTISIA, CONIUM MAC, ECHINACEA, EUPATORIUM PERF, SILICEA, THUJA OCC	Total Operations Management LLC DBA:Bestmade Natural Products Micro	540e4ee3-596f-4cea-e063-6294a90a6a60	2026-06-12	Warnings	Exact identifier unii: ETJ7Z6XBU4

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.