FDA.reportPublic FDA data

NDC 68437-010-20 - Sulfur

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
68437-010
Requested NDC
68437-010-20
Package NDCs from labels
68437-010-20, 68437-010-01
Manufacturer
GRISI Hnos, S.A DE C.V
Effective date
2022-10-14
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Sulfur - GRISI Hnos, S.A DE C.VGRISI Hnos, S.A DE C.V2022-10-14HUMAN OTC DRUG LABEL

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
SULFURACTIVE INGREDIENT70FD1KFU70SULFUR OINTMENT [GRISI HNOS, S.A DE C.V]2
SULFURACTIVE MOIETY70FD1KFU70SULFUR OINTMENT [GRISI HNOS, S.A DE C.V]2
BUTYLATED HYDROXYTOLUENEINACTIVE INGREDIENT1P9D0Z171KSULFUR OINTMENT [GRISI HNOS, S.A DE C.V]2
CETOSTEARYL ALCOHOLINACTIVE INGREDIENT2DMT128M1SSULFUR OINTMENT [GRISI HNOS, S.A DE C.V]2
DMDM HYDANTOININACTIVE INGREDIENTBYR0546TOWSULFUR OINTMENT [GRISI HNOS, S.A DE C.V]2
ISOPROPYL MYRISTATEINACTIVE INGREDIENT0RE8K4LNJSSULFUR OINTMENT [GRISI HNOS, S.A DE C.V]2
LANOLININACTIVE INGREDIENT7EV65EAW6HSULFUR OINTMENT [GRISI HNOS, S.A DE C.V]2
LANOLIN ALCOHOLSINACTIVE INGREDIENT884C3FA9HESULFUR OINTMENT [GRISI HNOS, S.A DE C.V]2
MENTHOLINACTIVE INGREDIENTL7T10EIP3ASULFUR OINTMENT [GRISI HNOS, S.A DE C.V]2
METHYLPARABENINACTIVE INGREDIENTA2I8C7HI9TSULFUR OINTMENT [GRISI HNOS, S.A DE C.V]2
MINERAL OILINACTIVE INGREDIENTT5L8T28FGPSULFUR OINTMENT [GRISI HNOS, S.A DE C.V]2
OLEYL ALCOHOLINACTIVE INGREDIENT172F2WN8DVSULFUR OINTMENT [GRISI HNOS, S.A DE C.V]2
POLYSORBATE 80INACTIVE INGREDIENT6OZP39ZG8HSULFUR OINTMENT [GRISI HNOS, S.A DE C.V]2
PROPYLENE GLYCOLINACTIVE INGREDIENT6DC9Q167V3SULFUR OINTMENT [GRISI HNOS, S.A DE C.V]2
PROPYLPARABENINACTIVE INGREDIENTZ8IX2SC1OHSULFUR OINTMENT [GRISI HNOS, S.A DE C.V]2
SORBITAN MONOPALMITATEINACTIVE INGREDIENT77K6Z421KUSULFUR OINTMENT [GRISI HNOS, S.A DE C.V]2
TROLAMINEINACTIVE INGREDIENT9O3K93S3TKSULFUR OINTMENT [GRISI HNOS, S.A DE C.V]2
WATERINACTIVE INGREDIENT059QF0KO0RSULFUR OINTMENT [GRISI HNOS, S.A DE C.V]2

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 2 of 219 · 4,373 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
La Vaquita New RegularMETHYL SALICYLATEDelon Laboratories (1990) Ltdd62186ac-afbb-443e-98c2-f0d122422a3c2026-09-01WarningsExact identifier
unii: L7T10EIP3A
ActivICEMENTHOLMedline Industries, LP834adeb9-38ad-0cfe-e053-2991aa0af82f2026-09-01WarningsExact identifier
unii: L7T10EIP3A
La Vaquita New ExtraMETHYL SALICYLATE, MENTHOLDelon Laboratories (1990) Ltd3097a01b-cee5-492f-b65a-63992fb28e3a2026-09-01WarningsExact identifier
unii: L7T10EIP3A
MUCINEX INSTASOOTHE SORE THROAT PLUS COUGH SUGAR FREEHEXYLRESORCINOL AND MENTHOLReckitt Benckiser LLC4a938e15-a996-8538-e063-6294a90ad4ee2026-09-01WarningsExact identifier
unii: L7T10EIP3A
Folliculitis Treatment CreamBENZOYL PEROXIDEGuangzhou Hechuang Commercial Service Co.,Ltd.5a93f753-eb7d-ad11-e063-6294a90a67782026-09-01WarningsExact identifier
application number: M006
AntisepticEUCALYPTOL, MENTHOL, METHYL SALICYLATE, THYMOLWALMART INC. (see also Equate)ceb125d9-8c1b-498c-b0f0-f18756ede4422026-09-01WarningsExact identifier
unii: L7T10EIP3A
INVISIBLE ACNE PATCHESSALICYLIC ACID 0.5%Global America Group LLC1527e15f-472f-4e05-adb6-c2e561f503cf2026-08-31WarningsExact identifier
application number: M006
Orajel 4X Medicated Toothache and Gum CreamBENZALKONIUM CHLORIDE, BENZOCAINE, MENTHOL, ZINC CHLORIDEChurch & Dwight Co., Inc.5a1c82b4-02b3-d456-e063-6294a90a16bb2026-08-31WarningsExact identifier
unii: L7T10EIP3A
Orajel 4X Medicated Toothache and Gum PM CreamBENZALKONIUM CHLORIDE, BENZOCAINE, MENTHOL, ZINC CHLORIDEChurch & Dwight Co., Inc.5a1cdaf4-3388-280c-e063-6294a90ac70f2026-08-31WarningsExact identifier
unii: L7T10EIP3A
REINREUDE SMELLING SALTSMENTHOL 15% SMELLING SALTSHubei Minxin Pharmaceutical Co., Ltd.5a539219-f9b8-5e94-e063-6294a90a25932026-08-31WarningsExact identifier
unii: L7T10EIP3A
SERYNTH SMELLING SALTSMENTHOL 15% SMELLING SALTSHubei Minxin Pharmaceutical Co., Ltd.5a5405f9-9881-e547-e063-6294a90a0d102026-08-31WarningsExact identifier
unii: L7T10EIP3A
EAYONYUMT NECK PAIN RELIEFMENTHOLWuhan Ruihengjie Technology Co., Ltd.5a450e68-07a7-a4bb-e063-6294a90a97c92026-08-30WarningsExact identifier
unii: L7T10EIP3A
EAYONYUM BACK PAIN RELIEVINGMENTHOLWuhan Ruihengjie Technology Co., Ltd.5a458280-4f9c-5af6-e063-6394a90acb2e2026-08-30WarningsExact identifier
unii: L7T10EIP3A
EAYONYUM KNEE PAIN RELIEVINGMENTHOLWuhan Ruihengjie Technology Co., Ltd.5a45d19f-c753-71eb-e063-6294a90a48052026-08-30WarningsExact identifier
unii: L7T10EIP3A
The Acne Spot TreatmentSALICYLIC ACID SPOTSpotless, Inc.4a1a3716-9eaf-6be4-e063-6294a90a31c32026-08-30WarningsExact identifier
application number: M006
SYLVIRENE SMELLING SALTSMENTHOL 15% SMELLING SALTSHubei Minxin Pharmaceutical Co., Ltd.5a4fd689-2113-f15a-e063-6394a90a45ad2026-08-30WarningsExact identifier
unii: L7T10EIP3A
Rhinoost SMELLING SALTSMENTHOL 15% SMELLING SALTSHubei Minxin Pharmaceutical Co., Ltd.5a296baa-c101-3192-e063-6394a90aa2b02026-08-29WarningsExact identifier
unii: L7T10EIP3A
LUCKSKY SMELLING SALTSMENTHOL 15% SMELLING SALTSHubei Minxin Pharmaceutical Co., Ltd.5a29ee19-8b6d-b4fa-e063-6394a90ad81d2026-08-29WarningsExact identifier
unii: L7T10EIP3A
Flobow SMELLING SALTSMENTHOL 15% SMELLING SALTSHubei Minxin Pharmaceutical Co., Ltd.5a2aa169-90b5-417f-e063-6394a90aa2782026-08-29WarningsExact identifier
unii: L7T10EIP3A
Hoxlbin SMELLING SALTSMENTHOL 15% SMELLING SALTSHubei Minxin Pharmaceutical Co., Ltd.5a17b116-d573-1c4a-e063-6394a90a499b2026-08-28WarningsExact identifier
unii: L7T10EIP3A

Reported adverse events (FAERS/openFDA)#

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