NDC 0008-0844-01 - Protonix 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: 0008-0844
Requested NDC: 0008-0844-01
Package NDCs from labels: 0008-0844-01, 0008-0844-02
Manufacturer: Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. | AndersonBrecon Inc. | Takeda GmbH
Effective date: 2026-05-18
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
PANTOPRAZOLE - Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. \| AndersonBrecon Inc. \| Takeda GmbH	Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. \| AndersonBrecon Inc. \| Takeda GmbH	2026-05-18	HUMAN PRESCRIPTION DRUG LABEL
Protonix Delayed-Release - Cardinal Health 107, LLC	Cardinal Health 107, LLC	2024-10-10	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
0008-0844-02	2024-01-30	C162847	48780-1	1030e364-f951-111a-e063-dadaa90a10e2	These highlights do not include all the information needed to use PROTONIX safely and effectively. See full prescribing information for PROTONIX. PROTONIX (pantoprazole sodium) delayed-release tablets, for oral use PROTONIX (pantoprazole sodium) for delayed-release oral suspension Initial U.S. approval: 2000

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0008-0844-01	ProtonixDelayed-Release	1 in 1 PACKET	GRANULE, DELAYED RELEASE	1		48
0008-0844-02	ProtonixDelayed-Release	30 in 1 CARTON	GRANULE, DELAYED RELEASE	30		48

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0008-0844	PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [WYETH PHARMACEUTICALS LLC, A SUBSIDIARY OF PFIZER INC.]	47	Current NDC, Legacy NDC, 2 package rows	20240719_08098cb2-c048-4640-f387-6beec4a38936.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0008-0844-01	EA - Each	0008-0844	a4a64248-a74b-44f3-85c5-bfd22d4cd462	1	2012-07-24
0008-0844-02	EA - Each	0008-0844	923dad3a-0648-4fe5-b4ea-526fe7657d8d	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
PANTOPRAZOLE SODIUM	ACTIVE INGREDIENT	6871619Q5X	PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [WYETH PHARMACEUTICALS INC., A SUBSIDIARY OF PFIZER INC.]	26
PANTOPRAZOLE	ACTIVE MOIETY	D8TST4O562	PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [WYETH PHARMACEUTICALS INC., A SUBSIDIARY OF PFIZER INC.]	26
CALCIUM STEARATE	INACTIVE INGREDIENT	776XM7047L	PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [WYETH PHARMACEUTICALS INC., A SUBSIDIARY OF PFIZER INC.]	26
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [WYETH PHARMACEUTICALS INC., A SUBSIDIARY OF PFIZER INC.]	26
CROSPOVIDONE	INACTIVE INGREDIENT	68401960MK	PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [WYETH PHARMACEUTICALS INC., A SUBSIDIARY OF PFIZER INC.]	26
FERRIC OXIDE YELLOW	INACTIVE INGREDIENT	EX438O2MRT	PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [WYETH PHARMACEUTICALS INC., A SUBSIDIARY OF PFIZER INC.]	26
HYPROMELLOSE 2910 (3 MPA.S)	INACTIVE INGREDIENT	0VUT3PMY82	PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [WYETH PHARMACEUTICALS INC., A SUBSIDIARY OF PFIZER INC.]	26
HYPROMELLOSE 2910 (5 MPA.S)	INACTIVE INGREDIENT	R75537T0T4	PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [WYETH PHARMACEUTICALS INC., A SUBSIDIARY OF PFIZER INC.]	26
HYPROMELLOSE 2910 (6 MPA.S)	INACTIVE INGREDIENT	0WZ8WG20P6	PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [WYETH PHARMACEUTICALS INC., A SUBSIDIARY OF PFIZER INC.]	26
MANNITOL	INACTIVE INGREDIENT	3OWL53L36A	PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [WYETH PHARMACEUTICALS INC., A SUBSIDIARY OF PFIZER INC.]	26
METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A	INACTIVE INGREDIENT	NX76LV5T8J	PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [WYETH PHARMACEUTICALS INC., A SUBSIDIARY OF PFIZER INC.]	26
POLYSORBATE 80	INACTIVE INGREDIENT	6OZP39ZG8H	PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [WYETH PHARMACEUTICALS INC., A SUBSIDIARY OF PFIZER INC.]	26
POVIDONE K25	INACTIVE INGREDIENT	K0KQV10C35	PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [WYETH PHARMACEUTICALS INC., A SUBSIDIARY OF PFIZER INC.]	26
POVIDONE K90	INACTIVE INGREDIENT	RDH86HJV5Z	PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [WYETH PHARMACEUTICALS INC., A SUBSIDIARY OF PFIZER INC.]	26
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [WYETH PHARMACEUTICALS INC., A SUBSIDIARY OF PFIZER INC.]	26
SODIUM CARBONATE	INACTIVE INGREDIENT	45P3261C7T	PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [WYETH PHARMACEUTICALS INC., A SUBSIDIARY OF PFIZER INC.]	26
SODIUM LAURYL SULFATE	INACTIVE INGREDIENT	368GB5141J	PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [WYETH PHARMACEUTICALS INC., A SUBSIDIARY OF PFIZER INC.]	26
TALC	INACTIVE INGREDIENT	7SEV7J4R1U	PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [WYETH PHARMACEUTICALS INC., A SUBSIDIARY OF PFIZER INC.]	26
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [WYETH PHARMACEUTICALS INC., A SUBSIDIARY OF PFIZER INC.]	26
TRIETHYL CITRATE	INACTIVE INGREDIENT	8Z96QXD6UM	PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [WYETH PHARMACEUTICALS INC., A SUBSIDIARY OF PFIZER INC.]	26
PANTOPRAZOLE SODIUM	ACTIVE INGREDIENT	6871619Q5X	PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [CARDINAL HEALTH]	8
PANTOPRAZOLE	ACTIVE MOIETY	D8TST4O562	PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [CARDINAL HEALTH]	8
CALCIUM STEARATE	INACTIVE INGREDIENT	776XM7047L	PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [CARDINAL HEALTH]	8
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [CARDINAL HEALTH]	8
CROSPOVIDONE	INACTIVE INGREDIENT	68401960MK	PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [CARDINAL HEALTH]	8
FERRIC OXIDE YELLOW	INACTIVE INGREDIENT	EX438O2MRT	PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [CARDINAL HEALTH]	8
HYPROMELLOSE 2910 (3 MPA.S)	INACTIVE INGREDIENT	0VUT3PMY82	PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [CARDINAL HEALTH]	8
HYPROMELLOSE 2910 (5 MPA.S)	INACTIVE INGREDIENT	R75537T0T4	PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [CARDINAL HEALTH]	8
HYPROMELLOSE 2910 (6 MPA.S)	INACTIVE INGREDIENT	0WZ8WG20P6	PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [CARDINAL HEALTH]	8
MANNITOL	INACTIVE INGREDIENT	3OWL53L36A	PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [CARDINAL HEALTH]	8
METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A	INACTIVE INGREDIENT	NX76LV5T8J	PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [CARDINAL HEALTH]	8
POLYSORBATE 80	INACTIVE INGREDIENT	6OZP39ZG8H	PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [CARDINAL HEALTH]	8
POVIDONE K25	INACTIVE INGREDIENT	K0KQV10C35	PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [CARDINAL HEALTH]	8
POVIDONE K90	INACTIVE INGREDIENT	RDH86HJV5Z	PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [CARDINAL HEALTH]	8
PROPYLENE GLYCOL	INACTIVE INGREDIENT	6DC9Q167V3	PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [CARDINAL HEALTH]	8
SODIUM CARBONATE	INACTIVE INGREDIENT	45P3261C7T	PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [CARDINAL HEALTH]	8
SODIUM LAURYL SULFATE	INACTIVE INGREDIENT	368GB5141J	PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [CARDINAL HEALTH]	8
TALC	INACTIVE INGREDIENT	7SEV7J4R1U	PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [CARDINAL HEALTH]	8
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [CARDINAL HEALTH]	8
TRIETHYL CITRATE	INACTIVE INGREDIENT	8Z96QXD6UM	PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) TABLET, DELAYED RELEASE PROTONIX DELAYED-RELEASE (PANTOPRAZOLE SODIUM) GRANULE, DELAYED RELEASE [CARDINAL HEALTH]	8

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 39 of 117 · 2,333 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Velvet Tinted Moisturizing Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	SKIN BOSS L.L.C.	35a871dc-a707-9963-e063-6294a90a4396	2025-12-15		Exact identifier unii: 15FIX9V2JP
Velvet NT Moisturizing Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	SKIN BOSS L.L.C.	35a8508d-7069-c2d6-e063-6394a90a6219	2025-12-15		Exact identifier unii: 15FIX9V2JP
Proper Protection Plus Primer NT	TITANIUM DIOXIDE, ZINC OXIDE	Skin & Proper LLC	3596fe93-836b-4f8e-e063-6294a90a674a	2025-12-15		Exact identifier unii: 15FIX9V2JP
Proper Protection Plus Primer Tinted	TITANIUM DIOXIDE, ZINC OXIDE	Skin & Proper LLC	359723bb-6152-9566-e063-6294a90a59e0	2025-12-15		Exact identifier unii: 15FIX9V2JP
Proper Protection Plus Primer NT	TITANIUM DIOXIDE, ZINC OXIDE	Skin & Proper LLC	3596cd73-0811-32bc-e063-6394a90ad132	2025-12-15		Exact identifier unii: 15FIX9V2JP
Proper Protection Plus Primer Tinted	TITANIUM DIOXIDE, ZINC OXIDE	Skin & Proper LLC	359782d7-6601-7d96-e063-6394a90af9dc	2025-12-15		Exact identifier unii: 15FIX9V2JP
Tinted Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	ESTHETICS BY RIKI LLC	37f1b692-0b80-0536-e063-6294a90ae863	2025-12-15		Exact identifier unii: 15FIX9V2JP
Tinted Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	ESTHETICS BY RIKI LLC	387d5194-bc12-68c1-e063-6394a90ab152	2025-12-15		Exact identifier unii: 15FIX9V2JP
Tinted Mineral Sun Protectant	TITANIUM DIOXIDE, ZINC OXIDE	PANDA PAMPERING LLC	387c23c2-a9f0-f484-e063-6394a90a4104	2025-12-15		Exact identifier unii: 15FIX9V2JP
Tinted Mineral Sun Protectant	TITANIUM DIOXIDE, ZINC OXIDE	PANDA PAMPERING LLC	387be96f-8cda-ce02-e063-6394a90abea5	2025-12-15		Exact identifier unii: 15FIX9V2JP
REJUVN8	TITANIUM DIOXIDE, ZINC OXIDE	FLEUR DE VIE LLC	37ede476-43b6-a7c8-e063-6294a90a3e8f	2025-12-15		Exact identifier unii: 15FIX9V2JP
REJUVN8	TITANIUM DIOXIDE, ZINC OXIDE	FLEUR DE VIE LLC	37efa5e1-e88e-d251-e063-6394a90a9371	2025-12-15		Exact identifier unii: 15FIX9V2JP
Non-Tinted Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	THE BEAUTY ROOM OC INC	3dd330bf-92e4-3664-e063-6294a90a0475	2025-12-15	Warnings	Exact identifier unii: 15FIX9V2JP
Tinted Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	THE BEAUTY ROOM OC INC	3dd37dd1-fd43-7af4-e063-6394a90ae3a0	2025-12-15	Warnings	Exact identifier unii: 15FIX9V2JP
Non-Tinted Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	THE BEAUTY ROOM OC INC	3dd3dcab-e9fb-0ef5-e063-6394a90acef1	2025-12-15	Warnings	Exact identifier unii: 15FIX9V2JP
Tinted Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	THE BEAUTY ROOM OC INC	3dd40a6a-d52e-ab87-e063-6294a90a966e	2025-12-15	Warnings	Exact identifier unii: 15FIX9V2JP
Mattifying Skin Primer	TITANIUM DIOXIDE, ZINC OXIDE	SKIN MAVEN	37662032-2842-1982-e063-6294a90a49a0	2025-12-15		Exact identifier unii: 15FIX9V2JP
Deluxe Lip Protection	TITANIUM DIOXIDE, ZINC OXIDE	BIOHEALTH PLUS LLC	37657895-5fec-82d0-e063-6294a90acf67	2025-12-15		Exact identifier unii: 15FIX9V2JP
Facial Mineral Fusion	TITANIUM DIOXIDE, ZINC OXIDE	IT INTELLIGENT TREATMENT LLC	35944621-e6fb-cd98-e063-6294a90aa641	2025-12-15		Exact identifier unii: 15FIX9V2JP
Mineral Mousse	TITANIUM DIOXIDE, ZINC OXIDE	CLARITY SKIN CARE STUDIO, INC.	35d00778-3857-ce8f-e063-6394a90ab375	2025-12-15		Exact identifier unii: 15FIX9V2JP

Reported adverse events (FAERS/openFDA)#

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