NDC 31722-342-01 - Naproxen

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: 31722-342
Requested NDC: 31722-342-01
Package NDCs from labels: 31722-342-10, 31722-342-50, 31722-342-01, 31722-342-05
Manufacturer: Camber Pharmaceuticals | Invagen Pharmaceuticals
Effective date: 2025-09-03
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Naproxen - Camber Pharmaceuticals \| Invagen Pharmaceuticals	Camber Pharmaceuticals \| Invagen Pharmaceuticals	2025-09-03	HUMAN PRESCRIPTION DRUG LABEL
NAPROXEN - DirectRX	DirectRX	2020-01-21	HUMAN PRESCRIPTION DRUG LABEL
Naproxen - St. Mary's Medical Park Pharmacy \| Invagen Pharmaceuticals	St. Mary's Medical Park Pharmacy \| Invagen Pharmaceuticals	2018-11-15	HUMAN PRESCRIPTION DRUG LABEL
Naproxen Tablets, USP	Blenheim Pharmacal, Inc.	2015-12-11	HUMAN PRESCRIPTION DRUG LABEL
Naproxen - State of Florida DOH Central Pharmacy	State of Florida DOH Central Pharmacy	2014-10-21	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, Related label table
NDC	Effective	Related label
31722-342-05	2025-09-05	Naproxen Tablets, USP
31722-342-50	2025-09-05	Naproxen Tablets, USP
31722-342-05	2019-11-13	Naproxen Tablets, USP
31722-342-50	2019-11-13	Naproxen Tablets, USP

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
31722-342	NAPROXEN TABLET [CAMBER PHARMACEUTICALS]	1	Legacy NDC	20120201_8dd7fade-d750-49ce-b798-a1d3615e57b7.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
31722-342-01	EA - Each	31722-342	985e3d05-aaab-4fb1-a08e-08608cdd8ce5	1	2012-07-24
31722-342-05	EA - Each	31722-342	bff54d3a-d4b3-408a-ad96-f3763180cf67	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
NAPROXEN	ACTIVE INGREDIENT	57Y76R9ATQ	NAPROXEN TABLET [BLENHEIM PHARMACAL, INC.]	2
NAPROXEN	ACTIVE INGREDIENT	57Y76R9ATQ	NAPROXEN TABLET [DIRECTRX]	2
NAPROXEN	ACTIVE INGREDIENT	57Y76R9ATQ	NAPROXEN TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]	2
NAPROXEN	ACTIVE MOIETY	57Y76R9ATQ	NAPROXEN TABLET [BLENHEIM PHARMACAL, INC.]	2
NAPROXEN	ACTIVE MOIETY	57Y76R9ATQ	NAPROXEN TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]	2
NAPROXEN	ACTIVE MOIETY	57Y76R9ATQ	NAPROXEN TABLET [DIRECTRX]	2
COLLOIDAL SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	NAPROXEN TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]	2
CROSCARMELLOSE SODIUM	INACTIVE INGREDIENT	M28OL1HH48	NAPROXEN TABLET [BLENHEIM PHARMACAL, INC.]	2
CROSCARMELLOSE SODIUM	INACTIVE INGREDIENT	M28OL1HH48	NAPROXEN TABLET [DIRECTRX]	2
CROSCARMELLOSE SODIUM	INACTIVE INGREDIENT	M28OL1HH48	NAPROXEN TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]	2
FERRIC OXIDE YELLOW	INACTIVE INGREDIENT	EX438O2MRT	NAPROXEN TABLET [BLENHEIM PHARMACAL, INC.]	2
FERRIC OXIDE YELLOW	INACTIVE INGREDIENT	EX438O2MRT	NAPROXEN TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]	2
FERRIC OXIDE YELLOW	INACTIVE INGREDIENT	EX438O2MRT	NAPROXEN TABLET [DIRECTRX]	2
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	NAPROXEN TABLET [BLENHEIM PHARMACAL, INC.]	2
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	NAPROXEN TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]	2
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	NAPROXEN TABLET [DIRECTRX]	2
POVIDONE	INACTIVE INGREDIENT	FZ989GH94E	NAPROXEN TABLET [BLENHEIM PHARMACAL, INC.]	2
POVIDONE	INACTIVE INGREDIENT	FZ989GH94E	NAPROXEN TABLET [DIRECTRX]	2
POVIDONES	INACTIVE INGREDIENT	FZ989GH94E	NAPROXEN TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]	2
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	NAPROXEN TABLET [BLENHEIM PHARMACAL, INC.]	2
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	NAPROXEN TABLET [DIRECTRX]	2
NAPROXEN	ACTIVE INGREDIENT	57Y76R9ATQ	NAPROXEN TABLET [ST. MARY'S MEDICAL PARK PHARMACY]	1
NAPROXEN	ACTIVE INGREDIENT	57Y76R9ATQ	NAPROXEN TABLET [CAMBER PHARMACEUTICALS]	1
NAPROXEN	ACTIVE MOIETY	57Y76R9ATQ	NAPROXEN TABLET [ST. MARY'S MEDICAL PARK PHARMACY]	1
NAPROXEN	ACTIVE MOIETY	57Y76R9ATQ	NAPROXEN TABLET [CAMBER PHARMACEUTICALS]	1
CROSCARMELLOSE SODIUM	INACTIVE INGREDIENT	M28OL1HH48	NAPROXEN TABLET [ST. MARY'S MEDICAL PARK PHARMACY]	1
CROSCARMELLOSE SODIUM	INACTIVE INGREDIENT	M28OL1HH48	NAPROXEN TABLET [CAMBER PHARMACEUTICALS]	1
FERRIC OXIDE RED	INACTIVE INGREDIENT	1K09F3G675	NAPROXEN TABLET [CAMBER PHARMACEUTICALS]	1
FERRIC OXIDE YELLOW	INACTIVE INGREDIENT	EX438O2MRT	NAPROXEN TABLET [CAMBER PHARMACEUTICALS]	1
FERRIC OXIDE YELLOW	INACTIVE INGREDIENT	EX438O2MRT	NAPROXEN TABLET [ST. MARY'S MEDICAL PARK PHARMACY]	1
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	NAPROXEN TABLET [ST. MARY'S MEDICAL PARK PHARMACY]	1
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	NAPROXEN TABLET [CAMBER PHARMACEUTICALS]	1
POVIDONE	INACTIVE INGREDIENT	FZ989GH94E	NAPROXEN TABLET [ST. MARY'S MEDICAL PARK PHARMACY]	1
POVIDONE	INACTIVE INGREDIENT	FZ989GH94E	NAPROXEN TABLET [CAMBER PHARMACEUTICALS]	1
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	NAPROXEN TABLET [ST. MARY'S MEDICAL PARK PHARMACY]	1
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	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 13 of 44 · 863 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Cervical Drops 5002	CERVICAL DROPS	Professional Complementary Health Formulas	edd5f196-1423-4d4c-a8c1-89427c4f387e	2026-01-08	Warnings	Exact identifier unii: ETJ7Z6XBU4
Asbestox 6005	ASBESTOX	Professional Complementary Health Formulas	90bc0d00-01e4-4134-809e-e216fd09852a	2026-01-08	Warnings	Exact identifier unii: ETJ7Z6XBU4
Ledum Combination 9257	LEDUM COMBINATION	Professional Complementary Health Formulas	38b89b32-4915-487d-8b2d-250123487b15	2026-01-08	Warnings	Exact identifier unii: ETJ7Z6XBU4
Fourth Chakra (Heart) 7304	FOURTH CHAKRA (HEART)	Professional Complementary Health Formulas	ef061447-42ae-43d0-b6f3-bf19a96ffe92	2026-01-08	Warnings	Exact identifier unii: ETJ7Z6XBU4
Spinal Drops 5025	SPINAL DROPS	Professional Complementary Health Formulas	ca6d7250-9c9e-40a6-8d41-88aba33d21dd	2026-01-08	Warnings	Exact identifier unii: ETJ7Z6XBU4
Anti-Scar Drops 2084	ANTI-SCAR DROPS	Professional Complementary Health Formulas	ad0e9159-ed68-48aa-a7d1-7ff5c32ec304	2026-01-08	Warnings	Exact identifier unii: ETJ7Z6XBU4
Fifth Chakra (Throat) 7305	FIFTH CHAKRA (THROAT)	Professional Complementary Health Formulas	b731f708-10a8-451f-8550-1e7302102b96	2026-01-08	Warnings	Exact identifier unii: ETJ7Z6XBU4
Sixth Chakra (Third Eye) 7306	SIXTH CHAKRA (THIRD EYE)	Professional Complementary Health Formulas	174024e7-e231-456c-bc00-48a358d7160a	2026-01-08	Warnings	Exact identifier unii: ETJ7Z6XBU4
Injury Drops 2034	INJURY DROPS	Professional Complementary Health Formulas	024011a0-6471-4016-86d4-19eeb21f0d82	2026-01-08	Warnings	Exact identifier unii: ETJ7Z6XBU4
Third Chakra (Solar Plexus) 7303	THIRD CHAKRA (SOLAR PLEXUS)	Professional Complementary Health Formulas	eea89c37-ab87-4cc7-8dfc-e7f42a580dd9	2026-01-08	Warnings	Exact identifier unii: ETJ7Z6XBU4 unii: 1K09F3G675
Lymphastat	BAPTISIA TINCTORIA, ECHINACEA (ANGUSTIFOLIA), LOBELIA INFLATA, LOMATIUM DISSECTUM, HYDRASTIS CANADENSIS, LUNG (SUIS), PHYTOLACCA DECANDRA, SYMPHYTUM OFFICINALE, ACONITUM NAPELLUS, ARSENICUM ALBUM, BELLADONNA, BRYONIA (ALBA), CAUSTICUM, EUPATORIUM PERFOLIATUM, FERRUM PHOSPHORICUM, GELSEMIUM SEMPERVIRENS, HYPERICUM PERFORATUM, KALI CARBONICUM, LACHESIS MUTUS, NATRUM SULPHURICUM, PHOSPHORUS, PULSATILLA (PRATENSIS), RHUS TOX, SILICEA, SULPHUR, PYROGENIUM	Energique, Inc.	ff95b833-3760-4e34-9636-90b423fc0d7b	2026-01-07	Warnings	Exact identifier unii: ETJ7Z6XBU4
Naproxen	NAPROXEN	Acella Pharmaceuticals, LLC	7e6f03fb-4b36-4418-9684-f45637abbb78	2026-01-05	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: 57Y76R9ATQ
Naproxen	NAPROXEN	PD-Rx Pharmaceuticals, Inc.	fa2fe6fd-c476-dd29-e053-6294a90a9e9e	2026-01-05	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 198014 unii: 57Y76R9ATQ
Parathyropar	SYMPHYTUM OFFICINALE, BARYTA CARBONICA, CALCAREA CARBONICA, CALCAREA PHOSPHORICA, HEKLA LAVA, MANGANUM METALLICUM, PARATHYROID GLAND (BOVINE), RHUS TOX, SILICEA	Energique, Inc.	6b098910-2f36-4757-a463-e01105340c43	2026-01-05	Warnings	Exact identifier unii: ETJ7Z6XBU4
VACC HC	ANTIMONIUM TARTARICUM, ARSENICUM ALBUM, BRYONIA (ALBA), ECHINACEA (ANGUSTIFOLIA), GELSEMIUM SEMPERVIRENS, HEPAR SUIS, HISTAMINUM HYDROCHLORICUM, HYOSCYAMUS NIGER, INFLUENZINUM, LEDUM PALUSTRE, MERCURIUS SOLUBILIS, MEZEREUM, NICOTINAMIDUM, HUMAN CORONAVIRUS (RNA), SENEGA OFFICINALIS, SILICEA, SPIGELIA ANTHELMIA, SULPHUR, THUJA OCCIDENTALIS, ZINCUM METALLICUM	Deseret Biologicals, Inc.	16d782b2-1bef-45e5-8a1d-721b1ffe5631	2026-01-05	Warnings	Exact identifier unii: ETJ7Z6XBU4
Naproxen	NAPROXEN	Northwind Health Company, LLC	0de6d673-fa76-e9c0-e063-6394a90a9ded	2026-01-01	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: 57Y76R9ATQ
NAPROXEN	NAPROXEN	Northwind Health Company, LLC	f32d755e-4984-ee40-e053-2995a90a4ebe	2026-01-01	Warnings	Exact identifier rxcui: 198014 unii: 57Y76R9ATQ
Naproxen	NAPROXEN	Northwind Health Company, LLC	fb07a76b-98ce-85dd-e053-6294a90aa6a8	2026-01-01	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 198014 unii: 57Y76R9ATQ
Naproxen	NAPROXEN	Northwind Health Company, LLC	ab6ec2c9-5df9-346c-e053-2a95a90ac81d	2026-01-01	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 198014 unii: 57Y76R9ATQ
Naproxen	NAPROXEN	Northwind Health Company, LLC	db478961-d984-7c8e-e053-2995a90a8a12	2026-01-01	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: 57Y76R9ATQ

Reported adverse events (FAERS/openFDA)#

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