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 10 of 44 · 863 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
MINIDROPS	LUBRICANT EYE DROPS	Optics Laboratory, Inc	c13c5f91-50df-471c-a7c9-1747a2ac1250	2026-02-03	Warnings	Exact identifier unii: FZ989GH94E
Mold, Yeast and Dust	ACREMONIUM STRICTUM, ADRENALINUM, ALLIUM CEPA, ALTERNARIA ALTERNATA, ARSENICUM IODATUM, ASPERGILLUS FUMIGATUS, ASPERGILLUS NIGER, AUREOBASIDIUM PULLULANS, CANDIDA ALBICANS, CLADOSPORIUM HERBARUM, COCKROACH, DERMATOPHAGOIDES FARINAE, EPICOCCUM PURPURASCENS, FUSARIUM SOLANI, HISTAMINUM HYDROCHLORICUM, LYCOPODIUM CLAVATUM, MUCOR CIRCINELLOIDES, NATRUM SULPHURICUM, RHIZOPUS STOLONIFER, SACCHAROMYCES CEREVISIAE, SILICEA	NaturalCare	e0f53f47-acd9-43e2-a7a2-2a500bc9dc1b	2026-02-03	Warnings	Exact identifier unii: ETJ7Z6XBU4
Aquavit 1	AQUAVIT 1	Uriel Pharmacy Inc.	2354fcfc-05a2-444a-ace4-b3df61413157	2026-02-02	Warnings	Exact identifier unii: 1K09F3G675
Naproxen	NAPROXEN	A-S Medication Solutions	4e97e645-552d-424b-990a-f94349a86f17	2026-01-30	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 198014 unii: 57Y76R9ATQ
Calamine	CALAMINE	AMERISOURCE BERGEN	90d9d908-57ea-4062-ade0-8a4888939c91	2026-01-29	Warnings, Adverse reactions	Exact identifier unii: 1K09F3G675
Naproxen	NAPROXEN	A-S Medication Solutions	000155a8-709c-44e5-a75f-cd890f3a7caf	2026-01-29	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 198014 unii: 57Y76R9ATQ
Naproxen	NAPROXEN	A-S Medication Solutions	d06db628-f6f0-48e2-b538-69c0837c49e3	2026-01-29	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 198014 unii: 57Y76R9ATQ
Naproxen	NAPROXEN	A-S Medication Solutions	9d28422f-6f25-4f14-9272-e0907c971f33	2026-01-29	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 198014 unii: 57Y76R9ATQ
Naproxen	NAPROXEN	Preferred Pharmaceuticals Inc.	87acd650-ea8a-4396-be72-5568c4b1755c	2026-01-23	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 198014 unii: 57Y76R9ATQ
BioMicroneedle PDRN Cream	SILICON DIOXIDE	Guangzhou Shengyanghui Industrial Trading Co., Ltd	48e2edae-94ea-c42e-e063-6394a90a907b	2026-01-21	Warnings	Exact identifier unii: ETJ7Z6XBU4
Inflammation I	ECHINACEA (ANGUSTIFOLIA), NASTURTIUM AQUATICUM, PHYTOLACCA DECANDRA, HYDRASTIS CANADENSIS, APIS MELLIFICA, BELLADONNA, FERRUM PHOSPHORICUM, NITRICUM ACIDUM, OLEANDER, SILICEA	BioActive Nutritional, Inc.	3cb12181-ae7e-45c7-a1b1-e1952f36f8c3	2026-01-21	Warnings	Exact identifier unii: ETJ7Z6XBU4
Naproxen and esomeprazole magnesium	NAPROXEN AND ESOMEPRAZOLE MAGNESIUM	Preferred Pharmaceuticals Inc.	b295a90e-320f-4414-b80a-d11f06c00c96	2026-01-20	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: 57Y76R9ATQ
DENTI BUONGIORNO PLAQUE CARE LEMON MINT TOOTH	SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE, TETRASODIUM PYROPHOSPHATE	ATOSAFE CO., Ltd	487c5036-0eb0-ada9-e063-6394a90aa02e	2026-01-16	Warnings	Exact identifier unii: ETJ7Z6XBU4
DENTI BUONGIORNO PLAQUE CARE LEMON MINT TOOTH	SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE, TETRASODIUM PYROPHOSPHATE	DONG IL PHARMS CO.,LTD	487cd5b9-28f3-392d-e063-6394a90a9ba1	2026-01-16	Warnings	Exact identifier unii: ETJ7Z6XBU4
DENTI BUONGIORNO GUM CARE COOL MINT TOOTH	SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE	ATOSAFE CO., Ltd	487cf27a-d761-6353-e063-6394a90af029	2026-01-16	Warnings	Exact identifier unii: ETJ7Z6XBU4
DENTI BUONGIORNO FRESH BREATH HERB MINT TOOTH	SILICA, SODIUM MONOFLUOROPHOSPHATE	ATOSAFE CO., Ltd	487d52d1-8853-bc90-e063-6394a90ab91d	2026-01-16	Warnings	Exact identifier unii: ETJ7Z6XBU4
DENTI BUONGIORNO GUM CARE COOL MINT TOOTH	SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE	DONG IL PHARMS CO.,LTD	487d689d-ebdd-43c3-e063-6294a90af0e2	2026-01-16	Warnings	Exact identifier unii: ETJ7Z6XBU4
DENTI BUONGIORNO FRESH BREATH HERB MINT TOOTH	SILICA, SODIUM MONOFLUOROPHOSPHATE	DONG IL PHARMS CO.,LTD	487da363-1d01-8cdc-e063-6294a90ac24d	2026-01-16	Warnings	Exact identifier unii: ETJ7Z6XBU4
Berberis Quartz	BERBERIS QUARTZ	Uriel Pharmacy Inc.	5da48d70-1140-495d-b672-0e55c04196e1	2026-01-16	Warnings	Exact identifier unii: ETJ7Z6XBU4
Constipation Relief	ALUMINUM OXIDE, BRYONIA ALBA ROOT, SODIUM CHLORIDE, GRAPHITE, SILICON DIOXIDE	Homeocare Laboratories	62374240-cd14-44e2-9405-5f8996faf047	2026-01-12	Warnings	Exact identifier unii: ETJ7Z6XBU4

Reported adverse events (FAERS/openFDA)#

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