Home NDC 68437-010-01 Sulfur
Product NDC 68437-010
Requested package NDC 68437-010-01
11-digit product format 684370010
Labeler code 68437
Product ID 68437-010_eb0475c6-c759-55a1-e053-2a95a90a69e9
Type HUMAN OTC DRUG
Nonproprietary name Sulfur
Dosage form OINTMENT
Route TOPICAL
Labeler GRISI Hnos, S.A DE C.V
Application M006
Marketing category OTC MONOGRAPH FINAL
Marketing start 2012-12-01
Marketing end 0000-00-00
Substance SULFUR
Active strength 10 g/100g
NDC exclude flag No
Listing certified through 2023-12-31
Current FDA listing Historical FDA.report record Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 1 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-01-11 03:41 UTC · source 2025-01-10 excluded package package 68437-010 68437-010-01 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded SULFUR ACTIVE INGREDIENT 70FD1KFU70 SULFUR OINTMENT [GRISI HNOS, S.A DE C.V] 2 SULFUR ACTIVE MOIETY 70FD1KFU70 SULFUR OINTMENT [GRISI HNOS, S.A DE C.V] 2 BUTYLATED HYDROXYTOLUENE INACTIVE INGREDIENT 1P9D0Z171K SULFUR OINTMENT [GRISI HNOS, S.A DE C.V] 2 CETOSTEARYL ALCOHOL INACTIVE INGREDIENT 2DMT128M1S SULFUR OINTMENT [GRISI HNOS, S.A DE C.V] 2 DMDM HYDANTOIN INACTIVE INGREDIENT BYR0546TOW SULFUR OINTMENT [GRISI HNOS, S.A DE C.V] 2 ISOPROPYL MYRISTATE INACTIVE INGREDIENT 0RE8K4LNJS SULFUR OINTMENT [GRISI HNOS, S.A DE C.V] 2 LANOLIN INACTIVE INGREDIENT 7EV65EAW6H SULFUR OINTMENT [GRISI HNOS, S.A DE C.V] 2 LANOLIN ALCOHOLS INACTIVE INGREDIENT 884C3FA9HE SULFUR OINTMENT [GRISI HNOS, S.A DE C.V] 2 MENTHOL INACTIVE INGREDIENT L7T10EIP3A SULFUR OINTMENT [GRISI HNOS, S.A DE C.V] 2 METHYLPARABEN INACTIVE INGREDIENT A2I8C7HI9T SULFUR OINTMENT [GRISI HNOS, S.A DE C.V] 2 MINERAL OIL INACTIVE INGREDIENT T5L8T28FGP SULFUR OINTMENT [GRISI HNOS, S.A DE C.V] 2 OLEYL ALCOHOL INACTIVE INGREDIENT 172F2WN8DV SULFUR OINTMENT [GRISI HNOS, S.A DE C.V] 2 POLYSORBATE 80 INACTIVE INGREDIENT 6OZP39ZG8H SULFUR OINTMENT [GRISI HNOS, S.A DE C.V] 2 PROPYLENE GLYCOL INACTIVE INGREDIENT 6DC9Q167V3 SULFUR OINTMENT [GRISI HNOS, S.A DE C.V] 2 PROPYLPARABEN INACTIVE INGREDIENT Z8IX2SC1OH SULFUR OINTMENT [GRISI HNOS, S.A DE C.V] 2 SORBITAN MONOPALMITATE INACTIVE INGREDIENT 77K6Z421KU SULFUR OINTMENT [GRISI HNOS, S.A DE C.V] 2 TROLAMINE INACTIVE INGREDIENT 9O3K93S3TK SULFUR OINTMENT [GRISI HNOS, S.A DE C.V] 2 WATER INACTIVE INGREDIENT 059QF0KO0R SULFUR 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 30 of 54 · 1,079 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 68437-010-01 68437001001 1 TUBE in 1 CARTON (68437-010-01) > 20 g in 1 TUBE (68437-010-20) 1 tube 2012-12-01 0000-00-00 No No Current