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 61 of 108 · 2,150 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Dolce and Gabbana Everlast Foundation SPF 20 01N Light	OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE, ZINC OXIDE	Dolce & Gabbana Beauty S.R.L	2ccf4e45-4cec-417d-9f4c-28f376025f1d	2025-07-25	Warnings	Exact identifier unii: 15FIX9V2JP
Sunscreen	TITANIUM DIOXIDE 6.8%	Baxter of California, LLC	146030bc-2bf4-25ea-e063-6294a90a4613	2025-07-24	Warnings	Exact identifier unii: 15FIX9V2JP
La Defense Broad Spectrum SPF 30 Mineral Sunscreen	ZINC OXIDE, TITANIUM DIOXIDE	Luzern Laboratories, Inc	3f00befa-415d-415d-89e1-6ba8770ba51e	2025-07-21	Warnings	Exact identifier unii: 15FIX9V2JP
Aller-Chord F	ACETALDEHYDE, ACETICUM AC, ARG NIT, CAFFEINUM, CALC SULPH, CITRICUM AC, CORTISONE ACETICUM, ECHINACEA PURP, FOLLICULINUM, FRAGARIA, FUMARICUM AC, GALLICUM AC, GLANDULA SUPRARENALIS SUIS, HEPAR SUIS, HISTAMINUM HYDROCHLORICUM, HYDRANGEA, LAC VAC, LECITHIN, LIMULUS, LYCOPERSICUM, LYCOPODIUM, NAT BICARB, NAT MUR, NUX VOM, PARAFFINUM, PHOSPHORICUM AC, SACCHARUM OFF, SILICEA, TARTARICUM AC, TORULA CEREVISIAE.	Energetix Corporation	ff4eb7b2-8272-4bd3-99a9-7e589b30d59a	2025-07-15	Warnings	Exact identifier unii: C151H8M554
Amarte ULTRA VEIL Daily	SUNSCREEN	Amarte USA LLC	39e9ca98-d0e8-6b8f-e063-6394a90aa366	2025-07-15	Warnings	Exact identifier unii: 15FIX9V2JP
Amarte ULTRA VEIL BB Fair	SUNSCREEN	Amarte USA LLC	39e87950-4103-c2eb-e063-6394a90a0552	2025-07-15	Warnings	Exact identifier unii: 15FIX9V2JP
Mineral Lip Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	CAPE COD SKIN CARE CO. INC.	39093b2d-3fbb-8378-e063-6294a90ac6d8	2025-07-03		Exact identifier unii: 15FIX9V2JP
Vertra S Dorian Kona Gold Signature Face Stick SPF 38	TITANIUM DIOXIDE	Toshiki Pigment Co., ltd.	b7162a2f-07f1-6188-e053-2995a90a8a9c	2025-06-27	Warnings	Exact identifier unii: 15FIX9V2JP
Steritalc 2g	TALC	Novatech SA	c94e51d9-beef-4b06-e053-2a95a90a754a	2025-06-25	Warnings, Adverse reactions	Exact identifier unii: 7SEV7J4R1U
MELAO WHITENING SUNSCREEN	TITANIUM DIOXIDE	Guangdong Aimu Biological Technology Co., Ltd	1aaf5942-ff13-ee07-e063-6394a90acd28	2025-06-25	Warnings	Exact identifier unii: 15FIX9V2JP
BISUTANG Sunscreen	BISUTANG SUNSCREEN	Guangdong Bisutang Biotechnology Co Ltd	37fdb01b-929e-6a60-e063-6394a90a94e0	2025-06-20		Exact identifier unii: 15FIX9V2JP
Double Use Compact SPF 15 gold deluxe edition Claire 1-2-3	OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE	Bel Star S.A. (Colombia)	b3747373-ef67-89ff-e053-2995a90afcde	2025-06-20	Warnings	Exact identifier unii: 15FIX9V2JP
LBEL DIVINE Double Use compact SPF 15 gold deluxe edition Obscure 8-9	ZINC OXIDE, TITANTIUM DIOXIDE, OCTINOXATE	Bel Star S.A. (Colombia)	b5e47c63-7e82-34fc-e053-2a95a90a767c	2025-06-20	Warnings	Exact identifier unii: 15FIX9V2JP
LipBOMB	TITANIUM DIOXIDE, ZINC OXIDE	FLEUR DE VIE LLC	37ef4c1e-2183-a277-e063-6394a90ae2df	2025-06-19		Exact identifier unii: 15FIX9V2JP
Tinted Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	ESTHETICS BY RIKI LLC	37f2c5ed-c2f5-e569-e063-6294a90a15b1	2025-06-19		Exact identifier unii: 15FIX9V2JP
Aloe UP SPF 30 Mineral	ZINC OXIDE, TITANIUM DIOXIDE	Aloe Care International, LLC	35967b33-bdfb-ee3c-e063-6294a90a75f6	2025-06-18	Warnings	Exact identifier unii: 15FIX9V2JP
Aloe Up SPF 50 Mineral	ZINC OXIDE, TITANIUM DIOXIDE	Aloe Care International, LLC	35b9dcfa-05f3-3d7b-e063-6394a90a18f1	2025-06-18	Warnings	Exact identifier unii: 15FIX9V2JP
Aloe Up SPF 50 Kids Mineral	ZINC OXIDE, TITANIUM DIOXIDE	Aloe Care International, LLC	35cd16b0-bd81-8f68-e063-6294a90a3d8c	2025-06-18	Warnings	Exact identifier unii: 15FIX9V2JP
Skin by Scottie Beach Mode Mineral Sunscreen Roll-On SPF 30	TITANIUM DIOXIDE, ZINC OXIDE	SKIN CARE BY SCOTTIE LLC	a9afa58c-f438-48c6-bd30-eda41334df74	2025-06-16	Warnings	Exact identifier unii: 15FIX9V2JP
Dermaka Sunscreen SPF 42, Tinted	TITANIUM DIOXIDE, ZINC OXIDE	DERMAKA SKIN PRODUCTS	9a967cd1-9eec-4255-b14b-ac2e33e4dbf0	2025-06-16	Warnings	Exact identifier unii: 15FIX9V2JP

Reported adverse events (FAERS/openFDA)#

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