NDC 51672-4111-01 - Phenytoin Sodium

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: 51672-4111
Requested NDC: 51672-4111-01
Package NDCs from labels: 51672-4111-6, 51672-4111-1, 51672-4111-3, 51672-4111-0, 51672-4111-01
Manufacturer: Major Pharmaceuticals
Effective date: 2026-08-20
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Phenytoin Sodium - Major Pharmaceuticals	Major Pharmaceuticals	2026-08-20	HUMAN PRESCRIPTION DRUG LABEL
Phenytoin Sodium - A-S Medication Solutions	A-S Medication Solutions	2026-07-24	HUMAN PRESCRIPTION DRUG LABEL
Phenytoin Sodium - REMEDYREPACK INC.	REMEDYREPACK INC.	2026-05-19	HUMAN PRESCRIPTION DRUG LABEL
Phenytoin Sodium - Coupler LLC	Coupler LLC	2026-05-13	HUMAN PRESCRIPTION DRUG LABEL
Phenytoin Sodium - Golden State Medical Supply, Inc.	Golden State Medical Supply, Inc.	2026-04-21	HUMAN PRESCRIPTION DRUG LABEL
Phenytoin Sodium - REMEDYREPACK INC.	REMEDYREPACK INC.	2026-03-25	HUMAN PRESCRIPTION DRUG LABEL
Phenytoin Sodium - Sun Pharmaceutical Industries, Inc. \| Taro Pharmaceutical Industries Ltd.,	Sun Pharmaceutical Industries, Inc. \| Taro Pharmaceutical Industries Ltd.,	2026-03-17	HUMAN PRESCRIPTION DRUG LABEL
Phenytoin Sodium - AvPAK	AvPAK	2026-03-03	HUMAN PRESCRIPTION DRUG LABEL
Phenytoin Sodium - Proficient Rx LP	Proficient Rx LP	2026-02-01	HUMAN PRESCRIPTION DRUG LABEL
Phenytoin Sodium - Aphena Pharma Solutions - Tennessee, LLC	Aphena Pharma Solutions - Tennessee, LLC	2024-12-20	HUMAN PRESCRIPTION DRUG LABEL
Phenytoin Sodium - NCS HealthCare of KY, LLC dba Vangard Labs	NCS HealthCare of KY, LLC dba Vangard Labs	2023-03-23	HUMAN PRESCRIPTION DRUG LABEL
Phenytoin Sodium - RPK Pharmaceuticals, Inc.	RPK Pharmaceuticals, Inc.	2020-12-25	HUMAN PRESCRIPTION DRUG LABEL
Phenytoin Sodium - Clinical Solutions Wholesale, LLC	Clinical Solutions Wholesale, LLC	2020-09-25	HUMAN PRESCRIPTION DRUG LABEL
Phenytoin Sodium - A-S Medication Solutions	A-S Medication Solutions	2018-07-06	HUMAN PRESCRIPTION DRUG LABEL
Phenytoin Sodium - TYA Pharmaceuticals	TYA Pharmaceuticals	2014-06-17	HUMAN PRESCRIPTION DRUG LABEL
Extended Phenytoin Sodium Capsules USP, 100 mg	Physicians Total Care, Inc.	2012-02-12	HUMAN PRESCRIPTION DRUG LABEL
Phenytoin Sodium - Rebel Distributors Corp	Rebel Distributors Corp	2011-01-04	HUMAN PRESCRIPTION DRUG LABEL
Phenytoin Sodium - Contract Pharmacy Services-PA	Contract Pharmacy Services-PA	2010-04-06	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
51672-4111-0	Phenytoin Sodium	10 in 1 CARTON	CAPSULE, EXTENDED RELEASE	10	16
51672-4111-0	Phenytoin Sodium	10 in 1 BLISTER PACK	CAPSULE, EXTENDED RELEASE	10	16
51672-4111-1	Phenytoin Sodium	100 in 1 BOTTLE	CAPSULE, EXTENDED RELEASE	100	16
51672-4111-3	Phenytoin Sodium	1000 in 1 BOTTLE	CAPSULE, EXTENDED RELEASE	1000	16
51672-4111-6	Phenytoin Sodium	30 in 1 BOTTLE	CAPSULE, EXTENDED RELEASE	30	16

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51672-4111	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [TARO PHARMACEUTICALS U.S.A., INC.]	15	Current NDC, Legacy NDC, 5 package rows	20240929_601f7353-225d-4a5d-9810-3869c2c21874.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
51672-4111-1	EA - Each	51672-4111	0f23fecb-57c3-4685-be86-4d4a9d0bae2b	1	2012-07-24
51672-4111-3	EA - Each	51672-4111	ce9b3ded-f89d-4b8d-8d40-286c6ac91bdb	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Phenytoin Sodium	ACTIVE INGREDIENT	4182431BJH	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [TARO PHARMACEUTICALS U.S.A., INC.]	7
Phenytoin	ACTIVE MOIETY	6158TKW0C5	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [TARO PHARMACEUTICALS U.S.A., INC.]	7
benzyl alcohol	INACTIVE INGREDIENT	LKG8494WBH	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [TARO PHARMACEUTICALS U.S.A., INC.]	7
butylparaben	INACTIVE INGREDIENT	3QPI1U3FV8	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [TARO PHARMACEUTICALS U.S.A., INC.]	7
D&C Yellow NO. 10	INACTIVE INGREDIENT	35SW5USQ3G	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [TARO PHARMACEUTICALS U.S.A., INC.]	7
edetate calcium disodium	INACTIVE INGREDIENT	25IH6R4SGF	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [TARO PHARMACEUTICALS U.S.A., INC.]	7
FD&C Red NO. 3	INACTIVE INGREDIENT	PN2ZH5LOQY	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [TARO PHARMACEUTICALS U.S.A., INC.]	7
gelatin	INACTIVE INGREDIENT	2G86QN327L	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [TARO PHARMACEUTICALS U.S.A., INC.]	7
hypromelloses	INACTIVE INGREDIENT	3NXW29V3WO	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [TARO PHARMACEUTICALS U.S.A., INC.]	7
lactose monohydrate	INACTIVE INGREDIENT	EWQ57Q8I5X	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [TARO PHARMACEUTICALS U.S.A., INC.]	7
magnesium stearate	INACTIVE INGREDIENT	70097M6I30	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [TARO PHARMACEUTICALS U.S.A., INC.]	7
methylparaben	INACTIVE INGREDIENT	A2I8C7HI9T	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [TARO PHARMACEUTICALS U.S.A., INC.]	7
propylparaben	INACTIVE INGREDIENT	Z8IX2SC1OH	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [TARO PHARMACEUTICALS U.S.A., INC.]	7
sodium lauryl sulfate	INACTIVE INGREDIENT	368GB5141J	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [TARO PHARMACEUTICALS U.S.A., INC.]	7
sodium propionate	INACTIVE INGREDIENT	DK6Y9P42IN	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [TARO PHARMACEUTICALS U.S.A., INC.]	7
SUCROSE	INACTIVE INGREDIENT	C151H8M554	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [TARO PHARMACEUTICALS U.S.A., INC.]	7
talc	INACTIVE INGREDIENT	7SEV7J4R1U	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [TARO PHARMACEUTICALS U.S.A., INC.]	7
titanium dioxide	INACTIVE INGREDIENT	15FIX9V2JP	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [TARO PHARMACEUTICALS U.S.A., INC.]	7
Phenytoin Sodium	ACTIVE INGREDIENT	4182431BJH	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [TYA PHARMACEUTICALS]	2
Phenytoin Sodium	ACTIVE INGREDIENT	4182431BJH	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [PHYSICIANS TOTAL CARE, INC.]	2
Phenytoin	ACTIVE MOIETY	6158TKW0C5	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [TYA PHARMACEUTICALS]	2
Phenytoin	ACTIVE MOIETY	6158TKW0C5	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [PHYSICIANS TOTAL CARE, INC.]	2
BENZYL ALCOHOL	INACTIVE INGREDIENT	LKG8494WBH	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [TYA PHARMACEUTICALS]	2
benzyl alcohol	INACTIVE INGREDIENT	LKG8494WBH	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [PHYSICIANS TOTAL CARE, INC.]	2
BUTYLPARABEN	INACTIVE INGREDIENT	3QPI1U3FV8	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [TYA PHARMACEUTICALS]	2
butylparaben	INACTIVE INGREDIENT	3QPI1U3FV8	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [PHYSICIANS TOTAL CARE, INC.]	2
D&C Yellow NO. 10	INACTIVE INGREDIENT	35SW5USQ3G	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [PHYSICIANS TOTAL CARE, INC.]	2
D&C YELLOW NO. 10	INACTIVE INGREDIENT	35SW5USQ3G	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [TYA PHARMACEUTICALS]	2
edetate calcium disodium	INACTIVE INGREDIENT	25IH6R4SGF	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [PHYSICIANS TOTAL CARE, INC.]	2
EDETATE CALCIUM DISODIUM	INACTIVE INGREDIENT	25IH6R4SGF	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [TYA PHARMACEUTICALS]	2
FD&C RED NO. 3	INACTIVE INGREDIENT	PN2ZH5LOQY	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [TYA PHARMACEUTICALS]	2
FD&C Red NO. 3	INACTIVE INGREDIENT	PN2ZH5LOQY	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [PHYSICIANS TOTAL CARE, INC.]	2
GELATIN	INACTIVE INGREDIENT	2G86QN327L	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [TYA PHARMACEUTICALS]	2
gelatin	INACTIVE INGREDIENT	2G86QN327L	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [PHYSICIANS TOTAL CARE, INC.]	2
HYPROMELLOSES	INACTIVE INGREDIENT	3NXW29V3WO	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [TYA PHARMACEUTICALS]	2
hypromelloses	INACTIVE INGREDIENT	3NXW29V3WO	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [PHYSICIANS TOTAL CARE, INC.]	2
lactose monohydrate	INACTIVE INGREDIENT	EWQ57Q8I5X	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [PHYSICIANS TOTAL CARE, INC.]	2
LACTOSE MONOHYDRATE	INACTIVE INGREDIENT	EWQ57Q8I5X	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [TYA PHARMACEUTICALS]	2
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [TYA PHARMACEUTICALS]	2
magnesium stearate	INACTIVE INGREDIENT	70097M6I30	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [PHYSICIANS TOTAL CARE, INC.]	2
methylparaben	INACTIVE INGREDIENT	A2I8C7HI9T	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [PHYSICIANS TOTAL CARE, INC.]	2
METHYLPARABEN	INACTIVE INGREDIENT	A2I8C7HI9T	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [TYA PHARMACEUTICALS]	2
propylparaben	INACTIVE INGREDIENT	Z8IX2SC1OH	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [PHYSICIANS TOTAL CARE, INC.]	2
PROPYLPARABEN	INACTIVE INGREDIENT	Z8IX2SC1OH	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [TYA PHARMACEUTICALS]	2
SODIUM LAURYL SULFATE	INACTIVE INGREDIENT	368GB5141J	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [TYA PHARMACEUTICALS]	2
sodium lauryl sulfate	INACTIVE INGREDIENT	368GB5141J	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [PHYSICIANS TOTAL CARE, INC.]	2
sodium propionate	INACTIVE INGREDIENT	DK6Y9P42IN	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [PHYSICIANS TOTAL CARE, INC.]	2
SODIUM PROPIONATE	INACTIVE INGREDIENT	DK6Y9P42IN	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [TYA PHARMACEUTICALS]	2
SUCROSE	INACTIVE INGREDIENT	C151H8M554	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [PHYSICIANS TOTAL CARE, INC.]	2
SUCROSE	INACTIVE INGREDIENT	C151H8M554	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [TYA PHARMACEUTICALS]	2
TALC	INACTIVE INGREDIENT	7SEV7J4R1U	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [TYA PHARMACEUTICALS]	2
talc	INACTIVE INGREDIENT	7SEV7J4R1U	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [PHYSICIANS TOTAL CARE, INC.]	2
titanium dioxide	INACTIVE INGREDIENT	15FIX9V2JP	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [PHYSICIANS TOTAL CARE, INC.]	2
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [TYA PHARMACEUTICALS]	2
Phenytoin Sodium	ACTIVE INGREDIENT	4182431BJH	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [CONTRACT PHARMACY SERVICES-PA]	1
Phenytoin Sodium	ACTIVE INGREDIENT	4182431BJH	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [REBEL DISTRIBUTORS CORP]	1
Phenytoin	ACTIVE MOIETY	6158TKW0C5	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [CONTRACT PHARMACY SERVICES-PA]	1
Phenytoin	ACTIVE MOIETY	6158TKW0C5	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [REBEL DISTRIBUTORS CORP]	1
benzyl alcohol	INACTIVE INGREDIENT	LKG8494WBH	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [REBEL DISTRIBUTORS CORP]	1
benzyl alcohol	INACTIVE INGREDIENT	LKG8494WBH	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [CONTRACT PHARMACY SERVICES-PA]	1
butylparaben	INACTIVE INGREDIENT	3QPI1U3FV8	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [CONTRACT PHARMACY SERVICES-PA]	1
butylparaben	INACTIVE INGREDIENT	3QPI1U3FV8	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [REBEL DISTRIBUTORS CORP]	1
D&C YELLOW NO. 10	INACTIVE INGREDIENT	35SW5USQ3G	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [REBEL DISTRIBUTORS CORP]	1
edetate calcium disodium	INACTIVE INGREDIENT	25IH6R4SGF	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [REBEL DISTRIBUTORS CORP]	1
edetate calcium disodium	INACTIVE INGREDIENT	25IH6R4SGF	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [CONTRACT PHARMACY SERVICES-PA]	1
FD&C RED NO. 3	INACTIVE INGREDIENT	PN2ZH5LOQY	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [REBEL DISTRIBUTORS CORP]	1
gelatin	INACTIVE INGREDIENT	2G86QN327L	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [REBEL DISTRIBUTORS CORP]	1
gelatin	INACTIVE INGREDIENT	2G86QN327L	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [CONTRACT PHARMACY SERVICES-PA]	1
HYPROMELLOSES	INACTIVE INGREDIENT	3NXW29V3WO	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [REBEL DISTRIBUTORS CORP]	1
lactose monohydrate	INACTIVE INGREDIENT	EWQ57Q8I5X	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [CONTRACT PHARMACY SERVICES-PA]	1
lactose monohydrate	INACTIVE INGREDIENT	EWQ57Q8I5X	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [REBEL DISTRIBUTORS CORP]	1
magnesium stearate	INACTIVE INGREDIENT	70097M6I30	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [REBEL DISTRIBUTORS CORP]	1
magnesium stearate	INACTIVE INGREDIENT	70097M6I30	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [CONTRACT PHARMACY SERVICES-PA]	1
methylparaben	INACTIVE INGREDIENT	A2I8C7HI9T	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [CONTRACT PHARMACY SERVICES-PA]	1
methylparaben	INACTIVE INGREDIENT	A2I8C7HI9T	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [REBEL DISTRIBUTORS CORP]	1
propylparaben	INACTIVE INGREDIENT	Z8IX2SC1OH	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [CONTRACT PHARMACY SERVICES-PA]	1
propylparaben	INACTIVE INGREDIENT	Z8IX2SC1OH	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [REBEL DISTRIBUTORS CORP]	1
sodium lauryl sulfate	INACTIVE INGREDIENT	368GB5141J	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [REBEL DISTRIBUTORS CORP]	1
sodium lauryl sulfate	INACTIVE INGREDIENT	368GB5141J	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [CONTRACT PHARMACY SERVICES-PA]	1
sodium propionate	INACTIVE INGREDIENT	DK6Y9P42IN	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [REBEL DISTRIBUTORS CORP]	1
sodium propionate	INACTIVE INGREDIENT	DK6Y9P42IN	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [CONTRACT PHARMACY SERVICES-PA]	1
SUCROSE	INACTIVE INGREDIENT	C151H8M554	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [REBEL DISTRIBUTORS CORP]	1
talc	INACTIVE INGREDIENT	7SEV7J4R1U	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [CONTRACT PHARMACY SERVICES-PA]	1
talc	INACTIVE INGREDIENT	7SEV7J4R1U	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [REBEL DISTRIBUTORS CORP]	1
titanium dioxide	INACTIVE INGREDIENT	15FIX9V2JP	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [REBEL DISTRIBUTORS CORP]	1
titanium dioxide	INACTIVE INGREDIENT	15FIX9V2JP	PHENYTOIN SODIUM CAPSULE, EXTENDED RELEASE [CONTRACT PHARMACY SERVICES-PA]	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 87 of 108 · 2,146 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Glyreg	ACETICUM ACIDUM, CACAO, MAGNESIA SULPHURICA, NATRUM SULPHURICUM, VERBASCUM THAPSUS, GLANDULA SUPRARENALIS SUIS, PANCREAS SUIS, CORTISONE ACETICUM, THYROIDINUM (SUIS), IODIUM, LYCOPODIUM CLAVATUM, PHOSPHORUS, RANUNCULUS BULBOSUS, SACCHARUM OFFICINALE, VANADIUM METALLICUM, ZINCUM METALLICUM, CHROMIUM ACIDUM, CULEX MUSCA	Deseret Biologicals, Inc	28e670ca-ed35-4256-af20-74c25dc18099	2024-04-23	Warnings	Exact identifier unii: C151H8M554
SPF30 Sunscreen Cariposa	TITANIUM DIOXIDE, ZINC OXIDE	Talent Brands Company LLC	37d696d9-f89d-498e-8fe9-1f08d05d7b61	2024-04-18	Warnings	Exact identifier unii: 15FIX9V2JP
Cetaphil Daily Facial Moisturizer with suncreen SPF 50	OCTINOXATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE, TITANIUM DIOXIDE	Galderma Laboratories, L.P.	6650d137-e69e-4ec2-8311-3de74bf21315	2024-04-17	Warnings	Exact identifier unii: 15FIX9V2JP
SPF 30 Mineral Sunscreen Cariposa	TITANIUM DIOXIDE, ZINC OXIDE	Talent Brands Company LLC	0bc21573-d302-4d85-8d8f-dca9a48e1f35	2024-04-17	Warnings	Exact identifier unii: 15FIX9V2JP
Phenytoin Sodium	PHENYTOIN SODIUM	Hikma Pharmaceuticals USA Inc.	035a8d4e-2063-4240-83cb-d7eebcabe301	2024-04-09	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: 4182431BJH
Phenytoin Sodium	PHENYTOIN SODIUM	Hikma Pharmaceuticals USA Inc.	8ad1be7b-a1a4-4a2a-bf9b-d22b350aa6e7	2024-04-09	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: 4182431BJH
RV Illuminance Serum Tint Broad Spectrum 15	FACE FOUNDATION WITH SPF	REVLON CONSUMER PR Consumer Products Corp	132aab60-da19-7079-e063-6394a90a1d76	2024-03-27	Warnings	Exact identifier unii: 15FIX9V2JP
RV Illuminance Serum Tint Broad Spectrum 15 Amber	FACE FOUNDATION WITH SPF	REVLON CONSUMER PR Consumer Products Corp	2a0ac71c-e53a-5ff9-e063-6394a90a4807	2024-03-27	Warnings	Exact identifier unii: 15FIX9V2JP
EltaMD UV Pure SPF47	ZINC OXIDE AND TITANIUM DIOXIDE SUNSCREEN	CP Skin Health Group, Inc.	9afe900b-4186-4189-a871-ad6f26fc26e4	2024-03-27	Warnings	Exact identifier unii: 15FIX9V2JP
Envirotox	TRITICUM AESTIVUM, BERBERIS VULGARIS, LAPPA MAJOR, RHAMNUS PURSHIANA, SENNS (CASSIA ANGUSTIFOLIA), PHYTOLACCA DECANDRA, GLYCYRRHIZA GLABRA, STILLINGIA SYLVATICA, TRIFOLIUM PRATENSE, XANTHOXYLUM FRAXINEUM, ACETONUM ACETONE, SODIUM TRIPOLYPHOSPHATE, PROPYLENE GLYCOL, BENZINUM, AMMONIUM MURIATICUM, SODIUM LAURYL SULFATE, TEREBINTHINA, BELLADONNA, LYCOPODIUM CLAVATUM, NITRICUM ACIDUM, NUX VOMICA, PHOSPHORICUM ACIDUM, BELLADONNA, LYCOPODIUM CLAVATUM, NITRICUM ACIDUM, NUX VOMICA, PHOSPHORICUM ACIDUM.	BioActive Nutritional, Inc.	2b5cfdba-cf4d-4eb0-8c60-20eac6922663	2024-03-26	Warnings	Exact identifier unii: 368GB5141J
SPF 50 Mineral Based Facial Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	Hutton, Kathleen MD	5cf0d2e3-d496-424c-ac75-70ff5b87e9ca	2024-03-25	Warnings	Exact identifier unii: 15FIX9V2JP
Daily Prevention Advanced Smartblend Mineral Moisturizer SPF 75	TITANIUM DIOXIDE AND ZINC OXIDE	Allure Labs	141bb721-cd1c-5bba-e063-6394a90ab8fa	2024-03-20	Warnings	Exact identifier unii: 15FIX9V2JP
Sunscreen-Lotion	ZINC OXIDE, TITANIUM DIOXIDE	Shanghai Chuangshi Medical Technology (Group) Co., Ltd.	0511ff57-b7bd-4708-e063-6294a90a58a8	2024-03-20	Warnings	Exact identifier unii: 15FIX9V2JP
Daily Prevention Pure Mineral Tinted Moisturizer SPF 30	TITANIUM DIOXIDE AND ZINC OXIDE	Allure Labs	13bc141b-a30f-2661-e063-6294a90aca2b	2024-03-15	Warnings	Exact identifier unii: 15FIX9V2JP
Habit	CHAMOMILLA, NATRUM PHOSPHORICUM, VALERIANA OFFICINALIS, PASSIFLORA INCARNATA, ARGENTUM NITRICUM, CALADIUM SEGUINUM, CINCHONA OFFICINALIS, MURIATICUM ACIDUM, SACCHARUM OFFICINALE, AVENA SATIVA, TABACUM, CEREBRUM SUIS, SEROTONIN (HYDROCHLORIDE), ARGEMONE MEXICANA, AGARICUS MUSCARIUS, ARSENICUM ALBUM, AURUM METALLICUM, IPECACUANHA, SEPIA, HYPOTHALAMUS (BOVINE), VIPERA BERUS	Deseret Biologicals, Inc.	3d00a305-e15d-4419-97bd-332421d4a1b0	2024-03-15	Warnings	Exact identifier unii: C151H8M554
BB Ambre 30 BS SPF30	ZINC OXIDE AND TITANIUM DIOXIDE	Allure Labs	13a3ec97-0d0a-d639-e063-6294a90a0bf8	2024-03-14	Warnings	Exact identifier unii: 15FIX9V2JP
Leaky Gut Formula	ALFALFA, GLYCYRRHIZA GLABRA, ASTACUS FLUVIATILIS, BERBERIS AQUIFOLIUM, LAC DEFLORATUM, NATRUM CARBONICUM, SACCHARUM OFFICINALE, ALOE, FEL TAURI, PANCREAS SUIS, FRAGARIA VESCA, ANTIMONIUM CRUDUM, CARBO VEGETABILIS, EUPHORBIUM OFFICINARUM, LYCOPODIUM CLAVATUM, MAGNESIA CARBONICA, ZINCUM METALLICUM, COLIBACILLINUM CUM NATRUM MURIATICUM, PROTEUS (VULGARIS)	Deseret Biologicals, Inc.	7e3a254b-a43d-43a2-a777-0d0c0057e131	2024-03-14	Warnings	Exact identifier unii: C151H8M554
BB Blanc 30 BS SPF30	ZINC OXIDE AND TITANIUM DIOXIDE	Allure Labs	137a1528-c487-8bf3-e063-6294a90ade84	2024-03-12	Warnings	Exact identifier unii: 15FIX9V2JP
BB Sienna 30 BS SPF30	ZINC OXIDE AND TITANIUM DIOXIDE	Allure Labs	137bff4a-5156-b12c-e063-6394a90abe63	2024-03-12	Warnings	Exact identifier unii: 15FIX9V2JP
BB Brite 30 BS SPF30	ZINC OXIDE AND TITANIUM DIOXIDE	Allure Labs	13660aee-3b28-7e3e-e063-6294a90a82cc	2024-03-11	Warnings	Exact identifier unii: 15FIX9V2JP

Reported adverse events (FAERS/openFDA)#

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