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 15 of 117 · 2,333 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Pantoprazole Sodium	PANTOPRAZOLE SODIUM	Cardinal Health 107, LLC	6b5ed424-2203-482f-bb85-2c97d9c356f2	2026-02-27	Warnings, Adverse reactions	Exact identifier rxcui: 314200 unii: 6871619Q5X
TIBENA EVERY DAY REAL SUN BLOCK	TITANIUM DIOXIDE, ZINC OXIDE	KONAD CO LTD	211c9930-4f91-cf8f-e063-6394a90a97b3	2026-02-26	Warnings	Exact identifier unii: 15FIX9V2JP
CLE DE PEAU BEAUTE RADIANT FLUID FOUNDATION MATTE M B10	TITANIUM DIOXIDE	Shiseido Americas Corporation	54f8210f-4934-4ada-89c3-aa89e7a09260	2026-02-26	Warnings	Exact identifier unii: 15FIX9V2JP
SHISEIDO UV PROTECTIVE COMPACT (REFILL) FAIR IVORY	OCTINOXATE, OCTOCRYLENE, AND TITANIUM DIOXIDE	SHISEIDO AMERICAS CORPORATION	c05cef12-a6a7-4682-9357-6d77f4ca3267	2026-02-25	Warnings	Exact identifier unii: 15FIX9V2JP
cle de peau BEAUTE RADIANT FOUNDATION N M I10	OCTINOXATE AND TITANIUM DIOXIDE	Shiseido Americas Corporation	3be1fe06-bd3b-4078-bee9-d3caf8d068ff	2026-02-25	Warnings	Exact identifier unii: 15FIX9V2JP
PANTOPRAZOLE SODIUM	PANTOPRAZOLE	PD-Rx Pharmaceuticals, Inc.	c1f37929-a981-4ace-95e6-ae6795a797b3	2026-02-25	Warnings, Adverse reactions	Exact identifier rxcui: 314200 unii: 6871619Q5X
cle de peau BEAUTE THE FOUNDATION N M O20	OCTINOXATE AND TITANIUM DIOXIDE	Shiseido Americas Corporation	9507f6d1-c11c-428d-8d95-b436f27ba26a	2026-02-24	Warnings	Exact identifier unii: 15FIX9V2JP
Perfect Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	SKIN PERFECT MEDICAL	4b93538a-3b3e-90f7-e063-6294a90ab898	2026-02-24	Warnings	Exact identifier unii: 15FIX9V2JP
ANTI-AGING TINTED SUNSCREEN	TITANIUM DIOXIDE, ZINC OXIDE	LASER GIRL SKINCARE, LLC	4b93cd22-1289-29bc-e063-6294a90ab781	2026-02-24	Warnings	Exact identifier unii: 15FIX9V2JP
ANTI-AGING TINTED SUNSCREEN	TITANIUM DIOXIDE, ZINC OXIDE	LASER GIRL SKINCARE, LLC	4b943d72-dcde-e2e4-e063-6294a90ab7c4	2026-02-24	Warnings	Exact identifier unii: 15FIX9V2JP
ANTI-AGING NON-TINTED SUNSCREEN	TITANIUM DIOXIDE, ZINC OXIDE	LASER GIRL SKINCARE, LLC	4b946c39-718b-d70e-e063-6394a90a0db8	2026-02-24	Warnings	Exact identifier unii: 15FIX9V2JP
SHISEIDO URBAN ENVIRONMENT MINERAL CLEAR SUNSCREEN	TITANIUM DIOXIDE, ZINC OXIDE	Shiseido Americas Corporation	b93f10dc-193d-4cda-94b6-3f0e54d89f21	2026-02-23	Warnings	Exact identifier unii: 15FIX9V2JP
SHISEIDO ULTIMATE SUN PROTECTOR MINERAL	TITANIUM DIOXIDE AND ZINC OXIDE	SHISEIDO AMERICAS CORPORATION	5e31eee8-6532-47ea-99fc-22418791804b	2026-02-23	Warnings	Exact identifier unii: 15FIX9V2JP
Perfect Mineral Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	SKIN PERFECT MEDICAL	4b47e7cb-17d6-6a7c-e063-6294a90abbea	2026-02-20	Warnings	Exact identifier unii: 15FIX9V2JP
Allay Skin Solutions Protect Nourish Mineral Sunscreen SPF 42	TITANIUM DIOXIDE, ZINC OXIDE	ALLAY SKIN SOLUTIONS LLC	425bf1d7-f2cf-4237-9047-dd53054acd1c	2026-02-18	Warnings	Exact identifier unii: 15FIX9V2JP
Hermes Plein Air-Baume de Teint Perfecteur Naturel-Enhancing Complexion Balm 85 TAMARIN	TITANIUM DIOXIDE	S.A. COMPTOIR NOUVEAU DE LA PARFUMERIE	dacff3dc-49d7-6416-e053-2a95a90a85c6	2026-02-18	Warnings	Exact identifier unii: 15FIX9V2JP
Pantoprazole Sodium	PANTOPRAZOLE SODIUM	Major Pharmaceuticals	9c286e5c-2b36-422b-9f74-e8c0abb3f747	2026-02-12	Warnings, Adverse reactions	Exact identifier rxcui: 314200 unii: 6871619Q5X
Alumier MD Clear Shield Broad Spectrum SPF 42 Sunscreen	TITANIUM DIOXIDE, ZINC OXIDE	Alumier Labs	a9c970c8-b6e3-b0a1-e053-2a95a90a89c7	2026-02-09	Warnings	Exact identifier unii: 15FIX9V2JP
Droptics Performance Eye Drops	NAPHAZOLINE HYDROCHLORIDE, PROPYLENE GLYCOL	Droptics LLC	20fd6822-a7fd-4593-92bb-0a07260893e2	2026-02-09	Warnings	Exact identifier unii: 6DC9Q167V3
Pantoprazole Sodium	PANTOPRAZOLE SODIUM	Aurobindo Pharma Limited	7418f358-f536-4de6-adf0-562b4373f2e3	2026-02-06	Warnings, Adverse reactions	Exact identifier rxcui: 251872 rxcui: 314200 unii: 6871619Q5X

Reported adverse events (FAERS/openFDA)#

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