NDC 0002-3240-01 - Cymbalta

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: 0002-3240
Requested NDC: 0002-3240-01
Package NDCs from labels: 0002-3240-30, 0002-3240-90, 0002-3240-01
Manufacturer: Eli Lilly and Company
Effective date: 2025-07-21
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Cymbalta - Eli Lilly and Company	Eli Lilly and Company	2025-07-21	HUMAN PRESCRIPTION DRUG LABEL
Cymbalta - PD-Rx Pharmaceuticals, Inc.	PD-Rx Pharmaceuticals, Inc.	2022-02-17	HUMAN PRESCRIPTION DRUG LABEL
Cymbalta - REMEDYREPACK INC.	REMEDYREPACK INC.	2021-07-01	HUMAN PRESCRIPTION DRUG LABEL
Cymbalta - Carilion Materials Management	Carilion Materials Management	2016-08-06	HUMAN PRESCRIPTION DRUG LABEL
Cymbalta - Aphena Pharma Solutions - Tennessee, LLC	Aphena Pharma Solutions - Tennessee, LLC	2014-04-14	HUMAN PRESCRIPTION DRUG LABEL
CYMBALTA - STAT Rx USA LLC \| PSS World Medical Inc.	STAT Rx USA LLC \| PSS World Medical Inc.	2012-02-24	HUMAN PRESCRIPTION DRUG LABEL
Cymbalta - Physicians Total Care, Inc.	Physicians Total Care, Inc.	2009-11-25	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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0002-3240-30	Cymbalta	30 in 1 BOTTLE	CAPSULE, DELAYED RELEASE	30		90
0002-3240-90	Cymbalta	90 in 1 BOTTLE	CAPSULE, DELAYED RELEASE	90		90

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0002-3240	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [ELI LILLY AND COMPANY]	89	Legacy NDC, 2 package rows	20241206_2f7d4d67-10c1-4bf4-a7f2-c185fbad64ba.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0002-3240-01	EA - Each	0002-3240	d2f4d6ed-bedf-4abf-8bab-e89fbba5b7ca	1	2012-07-24
0002-3240-30	EA - Each	0002-3240	645bd3f2-9265-4f93-9d12-cfd9af2c0a33	1	2012-07-24
0002-3240-33	EA - Each	0002-3240	f4beb227-97b9-4b44-995b-2edc68e3b833	1	2012-07-24
0002-3240-90	EA - Each	0002-3240	04b57d75-7338-4a24-9963-b562304535b8	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Duloxetine hydrochloride	ACTIVE INGREDIENT	9044SC542W	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [ELI LILLY AND COMPANY]	66
Duloxetine	ACTIVE MOIETY	O5TNM5N07U	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [ELI LILLY AND COMPANY]	66
FD&C BLUE NO. 2	INACTIVE INGREDIENT	L06K8R7DQK	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [ELI LILLY AND COMPANY]	66
FERRIC OXIDE YELLOW	INACTIVE INGREDIENT	EX438O2MRT	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [ELI LILLY AND COMPANY]	66
Gelatin	INACTIVE INGREDIENT	2G86QN327L	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [ELI LILLY AND COMPANY]	66
HYPROMELLOSE ACETATE SUCCINATE 16070722 (3 MM2/S)	INACTIVE INGREDIENT	24P2YXD2PW	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [ELI LILLY AND COMPANY]	66
Hypromelloses	INACTIVE INGREDIENT	3NXW29V3WO	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [ELI LILLY AND COMPANY]	66
Sodium lauryl sulfate	INACTIVE INGREDIENT	368GB5141J	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [ELI LILLY AND COMPANY]	66
Sucrose	INACTIVE INGREDIENT	C151H8M554	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [ELI LILLY AND COMPANY]	66
Talc	INACTIVE INGREDIENT	7SEV7J4R1U	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [ELI LILLY AND COMPANY]	66
Titanium dioxide	INACTIVE INGREDIENT	15FIX9V2JP	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [ELI LILLY AND COMPANY]	66
Triethyl citrate	INACTIVE INGREDIENT	8Z96QXD6UM	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [ELI LILLY AND COMPANY]	66
Duloxetine hydrochloride	ACTIVE INGREDIENT	9044SC542W	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [PD-RX PHARMACEUTICALS, INC.]	46
Duloxetine	ACTIVE MOIETY	O5TNM5N07U	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [PD-RX PHARMACEUTICALS, INC.]	46
FD&C BLUE NO. 2	INACTIVE INGREDIENT	L06K8R7DQK	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [PD-RX PHARMACEUTICALS, INC.]	46
Gelatin	INACTIVE INGREDIENT	2G86QN327L	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [PD-RX PHARMACEUTICALS, INC.]	46
HYPROMELLOSE ACETATE SUCCINATE 16070722 (3 MM2/S)	INACTIVE INGREDIENT	24P2YXD2PW	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [PD-RX PHARMACEUTICALS, INC.]	46
Hypromelloses	INACTIVE INGREDIENT	3NXW29V3WO	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [PD-RX PHARMACEUTICALS, INC.]	46
Sodium lauryl sulfate	INACTIVE INGREDIENT	368GB5141J	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [PD-RX PHARMACEUTICALS, INC.]	46
Sucrose	INACTIVE INGREDIENT	C151H8M554	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [PD-RX PHARMACEUTICALS, INC.]	46
Talc	INACTIVE INGREDIENT	7SEV7J4R1U	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [PD-RX PHARMACEUTICALS, INC.]	46
Titanium dioxide	INACTIVE INGREDIENT	15FIX9V2JP	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [PD-RX PHARMACEUTICALS, INC.]	46
Triethyl citrate	INACTIVE INGREDIENT	8Z96QXD6UM	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [PD-RX PHARMACEUTICALS, INC.]	46
Duloxetine hydrochloride	ACTIVE INGREDIENT	9044SC542W	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [CARILION MATERIALS MANAGEMENT]	2
Duloxetine hydrochloride	ACTIVE INGREDIENT	9044SC542W	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC]	2
Duloxetine	ACTIVE MOIETY	O5TNM5N07U	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC]	2
Duloxetine	ACTIVE MOIETY	O5TNM5N07U	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [CARILION MATERIALS MANAGEMENT]	2
FD&C BLUE NO. 2	INACTIVE INGREDIENT	L06K8R7DQK	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [CARILION MATERIALS MANAGEMENT]	2
FD&C BLUE NO. 2	INACTIVE INGREDIENT	L06K8R7DQK	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC]	2
GELATIN	INACTIVE INGREDIENT	2G86QN327L	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [CARILION MATERIALS MANAGEMENT]	2
Gelatin	INACTIVE INGREDIENT	2G86QN327L	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC]	2
HYPROMELLOSE ACETATE SUCCINATE 16070722 (3 MM2/S)	INACTIVE INGREDIENT	24P2YXD2PW	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC]	2
HYPROMELLOSE ACETATE SUCCINATE 16070722 (3 MM2/S)	INACTIVE INGREDIENT	24P2YXD2PW	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [CARILION MATERIALS MANAGEMENT]	2
Hypromelloses	INACTIVE INGREDIENT	3NXW29V3WO	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC]	2
HYPROMELLOSES	INACTIVE INGREDIENT	3NXW29V3WO	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [CARILION MATERIALS MANAGEMENT]	2
Sodium lauryl sulfate	INACTIVE INGREDIENT	368GB5141J	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC]	2
SODIUM LAURYL SULFATE	INACTIVE INGREDIENT	368GB5141J	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [CARILION MATERIALS MANAGEMENT]	2
Sucrose	INACTIVE INGREDIENT	C151H8M554	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC]	2
SUCROSE	INACTIVE INGREDIENT	C151H8M554	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [CARILION MATERIALS MANAGEMENT]	2
TALC	INACTIVE INGREDIENT	7SEV7J4R1U	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [CARILION MATERIALS MANAGEMENT]	2
Talc	INACTIVE INGREDIENT	7SEV7J4R1U	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC]	2
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [CARILION MATERIALS MANAGEMENT]	2
Titanium dioxide	INACTIVE INGREDIENT	15FIX9V2JP	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC]	2
TRIETHYL CITRATE	INACTIVE INGREDIENT	8Z96QXD6UM	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [CARILION MATERIALS MANAGEMENT]	2
Triethyl citrate	INACTIVE INGREDIENT	8Z96QXD6UM	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC]	2
DULOXETINE HYDROCHLORIDE	ACTIVE INGREDIENT	9044SC542W	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [STAT RX USA LLC]	1
DULOXETINE HYDROCHLORIDE	ACTIVE INGREDIENT	9044SC542W	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [PHYSICIANS TOTAL CARE, INC.]	1
DULOXETINE	ACTIVE MOIETY	O5TNM5N07U	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [STAT RX USA LLC]	1
DULOXETINE	ACTIVE MOIETY	O5TNM5N07U	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [PHYSICIANS TOTAL CARE, INC.]	1
FD&C BLUE NO. 2	INACTIVE INGREDIENT	L06K8R7DQK	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [PHYSICIANS TOTAL CARE, INC.]	1
FD&C BLUE NO. 2	INACTIVE INGREDIENT	L06K8R7DQK	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [STAT RX USA LLC]	1
FERRIC OXIDE YELLOW	INACTIVE INGREDIENT	EX438O2MRT	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [PHYSICIANS TOTAL CARE, INC.]	1
GELATIN	INACTIVE INGREDIENT	2G86QN327L	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [PHYSICIANS TOTAL CARE, INC.]	1
GELATIN	INACTIVE INGREDIENT	2G86QN327L	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [STAT RX USA LLC]	1
HYPROMELLOSE	INACTIVE INGREDIENT	3NXW29V3WO	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [PHYSICIANS TOTAL CARE, INC.]	1
HYPROMELLOSE ACETATE SUCCINATE 16070722 (3 MM2/S)	INACTIVE INGREDIENT	24P2YXD2PW	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [PHYSICIANS TOTAL CARE, INC.]	1
HYPROMELLOSE ACETATE SUCCINATE 16070722 (3 MM2/S)	INACTIVE INGREDIENT	24P2YXD2PW	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [STAT RX USA LLC]	1
HYPROMELLOSES	INACTIVE INGREDIENT	3NXW29V3WO	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [STAT RX USA LLC]	1
SODIUM LAURYL SULFATE	INACTIVE INGREDIENT	368GB5141J	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [PHYSICIANS TOTAL CARE, INC.]	1
SODIUM LAURYL SULFATE	INACTIVE INGREDIENT	368GB5141J	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [STAT RX USA LLC]	1
SUCROSE	INACTIVE INGREDIENT	C151H8M554	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [PHYSICIANS TOTAL CARE, INC.]	1
SUCROSE	INACTIVE INGREDIENT	C151H8M554	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [STAT RX USA LLC]	1
TALC	INACTIVE INGREDIENT	7SEV7J4R1U	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [STAT RX USA LLC]	1
TALC	INACTIVE INGREDIENT	7SEV7J4R1U	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [PHYSICIANS TOTAL CARE, INC.]	1
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [STAT RX USA LLC]	1
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [PHYSICIANS TOTAL CARE, INC.]	1
TRIETHYL CITRATE	INACTIVE INGREDIENT	8Z96QXD6UM	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [STAT RX USA LLC]	1
TRIETHYL CITRATE	INACTIVE INGREDIENT	8Z96QXD6UM	CYMBALTA (DULOXETINE HYDROCHLORIDE) CAPSULE, DELAYED RELEASE [PHYSICIANS TOTAL CARE, INC.]	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 57 of 111 · 2,207 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
e l f Camo Semi Matte CC SPF 30 Deep 530 W	ZINC OXIDE, TITANIUM DIOXIDE, HOMOSALATE, OCTISALATE, OCTOCRYLENE	e.l.f. Cosmetics, Inc.	940e0b2d-0b10-4534-ba36-e9980cead492	2025-10-21	Warnings	Exact identifier unii: 15FIX9V2JP
Sugar Cravings	CINNAMIC ACID, PHLORIDZINUM, ARGENTUM NITRICUM, ADENOSINUM TRIPHOSPHORICUM DINATRUM, BEET SUGAR, DEXTROSE, D-RIBOSE, FRUCTOSE, LYCOPODIUM CLAVATUM, MAPLE SUGAR, SACCHARUM LACTIS, SACCHARUM OFFICINALE, SARCOLACTICUM ACIDUM, MALVIN, ADRENOCORTICOTROPHIN, DYSENTERY BACILLUS, MORGAN GAERTNER	Dr. Donna Restivo DC	401873ba-ae1b-4506-a2e8-c6c0e5ff27f5	2025-10-21	Warnings	Exact identifier unii: C151H8M554
Clinical Skin Filter Tinted Sunscreen	CLINICAL SKIN FILTER TINTED SUNSCREEN	KRX RESOURCES SDN. BHD.	22b8856b-671f-def3-e063-6394a90a4ea0	2025-10-18	Warnings	Exact identifier unii: 15FIX9V2JP
Clinical Skin Filter Tinted Sunscreen Medium Dark	CLINICAL SKIN FILTER TINTED SUNSCREEN MEDIUM DARK	KRX RESOURCES SDN. BHD.	22cead37-f862-e859-e063-6394a90a86ce	2025-10-18	Warnings	Exact identifier unii: 15FIX9V2JP
Krx Aesthetics All Day Glow Sunblocker	KRX AESTHETICS ALL DAY GLOW SUNBLOCKER	KRX RESOURCES SDN. BHD.	22a60fb9-0fea-92c0-e063-6394a90a088c	2025-10-18	Warnings	Exact identifier unii: 15FIX9V2JP
DD Cream	DD CREAM	DERMAdoctor, Inc.	08c9a0cf-ee78-483b-e054-00144ff88e88	2025-10-16	Warnings	Exact identifier unii: 15FIX9V2JP
Ciele Filter and Protect	TITANIUM DIOXIDE, ZINC OXIDE	Ciele	0309b0ef-baca-b41d-e063-6294a90a49d7	2025-10-15	Warnings	Exact identifier unii: 15FIX9V2JP
Defend and Balance TInted Mineral Sunscreen SPF 50	SUNSCREEN	Epicuren Discovery	41367f05-59d8-6736-e063-6394a90a5f17	2025-10-15	Warnings	Exact identifier unii: 15FIX9V2JP
Duloxetine	DULOXETINE	Aphena Pharma Solutions - Tennessee, LLC	4121bd3f-2d6d-3bdd-e063-6294a90a3088	2025-10-14	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 596930 unii: 9044SC542W
Skinlycious Multi Protection Mineral Sunscreen Broad Spectrum SPF 30	TITANIUM DIOXIDE , ZINC OXIDE	Skinlycious Pte Ltd	e0ad02c3-f5ed-4b72-ba96-07d9c489a4ea	2025-10-13	Warnings	Exact identifier unii: 15FIX9V2JP
Vertra S Dorian Kona Gold Signature Face Stick SPF 38	TITANIUM DIOXIDE	Eai-jr 286, Inc	b6c316c3-661b-6428-e053-2a95a90a1a6b	2025-10-10	Warnings	Exact identifier unii: 15FIX9V2JP
Duloxetine	DULOXETINE	Quallent Pharmaceuticals Health LLC	b3b26383-9924-40f9-b4bb-43e30b70493e	2025-10-10	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 596926 rxcui: 596930 rxcui: 596934 unii: 9044SC542W
Dr Lift Mineral SPF 50	TITANIUM DIOXIDE, ZINC OXIDE	Spa de Soleil	40c03d65-8d09-371a-e063-6294a90a7ac6	2025-10-09	Warnings	Exact identifier unii: 15FIX9V2JP
Dr Lift Mineral SPF 30	TITANIUM DIOXIDE	Spa de Soleil	40c0e0d2-2c1d-e629-e063-6394a90a5aaf	2025-10-09	Warnings	Exact identifier unii: 15FIX9V2JP
Essential Defense Mineral Shield Broad Spectrum SPF 35 Sunscreen	TITANIUM DIOXIDE AND ZINC OXIDE	Allergan, Inc.	29817fdc-f14c-4013-a8ed-4367f3b2867c	2025-10-09	Warnings	Exact identifier unii: 15FIX9V2JP
Vertra Pearl White Face Stick SPF 50	PADIMATE O, TITANIUM DIOXIDE	Eai-jr 286, Inc	b69a75e0-8724-35ae-e053-2a95a90a5f34	2025-10-07	Warnings	Exact identifier unii: 15FIX9V2JP
Vertra Mick Fanning Signature Foundation Sunscreen Face Stick SPF 35 Coolangatta Beige	TITANIUM DIOXIDE	EAI-JR 286, Inc.	b9ea12e8-6ed9-d805-e053-2a95a90aa107	2025-10-07	Warnings	Exact identifier unii: 15FIX9V2JP
SPF50 Sunscreen	SUNSCREEN	KINGKEY MBC LIFE TECHNOLOGY GROUP CO., LTD	b3cde609-7d62-2ac7-e053-2a95a90a26b3	2025-10-07		Exact identifier unii: 15FIX9V2JP
Vertra Mick Fanning Signature Foundation Sunscreen Face Stick SPF 35 Coolangatta Beige	TITANIUM DIOXIDE	Toshiki Pigment Co., Ltd.	b9eba15f-493a-43c9-e053-2995a90a0451	2025-10-06	Warnings	Exact identifier unii: 15FIX9V2JP
PURE SOL SPF 37 Tinted Moisturizer	ZINC OXIDE TITANIUM DIOXIDE	Brand 2022b LLC	4052c4e4-2105-80c0-e063-6294a90af41d	2025-10-04	Warnings	Exact identifier unii: 15FIX9V2JP

Reported adverse events (FAERS/openFDA)#

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