NDC 70710-1233-01 - Betamethasone dipropionate

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: 70710-1233
Requested NDC: 70710-1233-01
Package NDCs from labels: 70710-1233-1, 70710-1233-4, 70710-1233-01
Manufacturer: REMEDYREPACK INC.
Effective date: 2025-07-25
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Betamethasone dipropionate - REMEDYREPACK INC.	REMEDYREPACK INC.	2025-07-25	HUMAN PRESCRIPTION DRUG LABEL
Betamethasone dipropionate - A-S Medication Solutions	A-S Medication Solutions	2023-12-15	HUMAN PRESCRIPTION DRUG LABEL
Betamethasone dipropionate - A-S Medication Solutions	A-S Medication Solutions	2023-10-31	HUMAN PRESCRIPTION DRUG LABEL
BETAMETHASONE - Zydus Pharmaceuticals USA Inc. \| Zydus Lifesciences Limited	Zydus Pharmaceuticals USA Inc. \| Zydus Lifesciences Limited	2022-10-05	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
70710-1233-1	Betamethasone dipropionate	15 g in 1 TUBE	CREAM	15	3
70710-1233-1	Betamethasone dipropionate	1 in 1 CARTON	CREAM	1	3
70710-1233-4	Betamethasone dipropionate	1 in 1 CARTON	CREAM	1	3
70710-1233-4	Betamethasone dipropionate	45 g in 1 TUBE	CREAM	45	3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70710-1233	BETAMETHASONE DIPROPIONATE CREAM [ZYDUS PHARMACEUTICALS USA INC.]	3	Current NDC, Legacy NDC, 4 package rows	20221007_18d80661-72ad-4a83-917f-a80ce37a5568.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
70710-1233-1	GM - Gram	70710-1233	76e92d62-4588-4356-b5ae-513a2a3f2635	1	2019-05-02
70710-1233-4	GM - Gram	70710-1233	ae208291-c0e1-424c-a37c-ce2ac84eac86	1	2019-05-02

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 37 of 43 · 847 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Mayinglong Hemorrhoidal	PETROLATUM, ZINC OXIDE	Mayinglong Pharmaceutical Group Co., Ltd.	b14192ea-1bf7-da6a-e053-2a95a90a5b5e	2023-12-08	Warnings	Exact identifier unii: 4T6H12BN9U
Calcipotriene and Betamethasone Dipropionate	CALCIPOTRIENE, BETAMETHASONE DIPROPIONATE	Bryant Ranch Prepack	174c5378-f2b9-4e9e-931a-4123137be62d	2023-12-07	Warnings, Adverse reactions	Exact identifier unii: 826Y60901U
Hemorrhoidal Pain Relief	MINERAL OIL, PETROLATUM, PHENYLEPHRINE HCL	WALGREENS	03bc5c1a-d493-5082-e063-6394a90ae87b	2023-12-05	Warnings	Exact identifier unii: 4T6H12BN9U unii: T5L8T28FGP
Welmedix HomeCare PRO Fragile Skin Protectant	PETROLATUM	Welmedix LLC	6e8d7151-c7fc-4b8f-9343-4a9f0f4e37cf	2023-12-05	Warnings	Exact identifier unii: 4T6H12BN9U
Welmedix HomeCare PRO Extra Strength Rapid Rash Relief	PETROLATUM, ZINC OXIDE	Welmedix LLC	551e6cce-7adc-4e98-baff-2703b83d7526	2023-12-05	Warnings	Exact identifier unii: 4T6H12BN9U
Hemorrhoidal Pain Relief Cream	GLYCERIN, PHENYLEPHRINE HCL, PRAMOXINE HCL, WHITE PETROLATUM	WALGREENS	03bbe146-f185-bcfa-e063-6394a90a85bf	2023-12-04	Warnings	Exact identifier unii: 4T6H12BN9U
Eye Wash	WATER	Jiangxi Zhenmei Biological Technology Co.,Ltd	c68795b8-bf68-0d01-e053-2a95a90abebb	2023-12-04	Warnings	Exact identifier unii: 059QF0KO0R
Petrolatum Jelly	PETROLATUM	NEW PRIDE CORP	f6634410-fa1f-7987-e053-2995a90abb06	2023-12-01	Warnings	Exact identifier unii: 4T6H12BN9U
Bloop Hemorrhoid Relief Topical	GLYCERIN, PETROLATUM, PHENYLEPHRINE HCL, PRAMOXINE HCL	Three Nations Corp	0b6419e3-f1c7-bdfe-e063-6294a90a5d92	2023-11-30	Warnings	Exact identifier unii: 4T6H12BN9U
Wynzora	CALCIPOTRIENE AND BETAMETHASONE DIPROPIONATE	MC2 Therapeutics Ltd	36c5c818-0d40-445e-a3c0-0f46723a25e2	2023-11-29	Warnings, Adverse reactions	Exact identifier unii: 826Y60901U
Betamethasone Dipropionate	BETAMETHASONE DIPROPIONATE	Cosette Pharmaceuticals, Inc.	4cc3b34f-9120-3362-0932-42d7024c8f89	2023-11-22	Adverse reactions	Exact identifier rxcui: 238920 unii: 826Y60901U
Sun X SPF 50 Broad Spectrum Sunscreen Lip Balm	AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, PETROLATUM	CoreTex Products, INC	c0355990-b842-47cd-e053-2a95a90a7c82	2023-11-20	Warnings	Exact identifier unii: 4T6H12BN9U
UNIVERSAL ORIGINAL PETROLEUM	WHITE PETROLEUM	Universal Distribution Center LLC	47b8c720-ad1e-4ac7-ba73-872e409b38bf	2023-11-17	Warnings	Exact identifier unii: 4T6H12BN9U
UNIVERSAL LAVENDER SCENT PETROLEUM	WHITE PETROLEUM	Universal Distribution Center LLC	1ac9ee69-339d-4426-b3bf-13e5386f1a9b	2023-11-17	Warnings	Exact identifier unii: 4T6H12BN9U
UNIVERSAL COCOA BUTTER SCENT PETROLEUM	WHITE PETROLEUM	Universal Distribution Center LLC	cf888bf3-6950-43aa-b4be-5a32961b4d96	2023-11-15	Warnings	Exact identifier unii: 4T6H12BN9U
UNIVERSAL BABY FRESH SCENT PETROLEUM	WHITE PETROLEUM	Universal Distribution Center LLC	b6e0ddb8-3761-482a-83d0-15d612d142eb	2023-11-15	Warnings	Exact identifier unii: 4T6H12BN9U
EltaMD Laser Balm	PETROLATUM SKIN PROTECTANT	CP Skin Health Group, Inc	1c67ce72-89d9-4c4f-a9b0-28b7e67d30eb	2023-11-09	Warnings	Exact identifier unii: 4T6H12BN9U
Jack Black Intense Therapy Lip Balm Passion Fruit	AVOBENZONE, OCTINOXATE LIP BALM SUNSCREEN	Jack Black, LLC	f34beb68-e5dc-45c4-a6d1-e9a031016228	2023-11-08	Warnings	Exact identifier unii: 4T6H12BN9U
Skin-lube	PETROLATUM, DIMETHICONE	The Hygenic Company, LLC.	d1005dec-04f6-3f88-e053-2a95a90ad9cb	2023-11-05	Warnings	Exact identifier unii: 4T6H12BN9U
Betamethasone dipropionate	BETAMETHASONE DIPROPIONATE	A-S Medication Solutions	1c15cbe5-51d6-4a1a-bb42-811f1d84ae66	2023-10-31	Adverse reactions	Exact identifier application number: ANDA208885 ndc (package): 50090-4680-0 ndc (product): 50090-4680 rxcui: 238920 spl id: 38ac25fc-2057-49f3-aa92-5e81e0416bcb spl set id: 1c15cbe5-51d6-4a1a-bb42-811f1d84ae66 unii: 826Y60901U

Reported adverse events (FAERS/openFDA)#

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