Home NDC 68437-010 Sulfur
Product NDC 68437-010
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 · 2 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 product product 68437-010 U Excluded because listing certification expired excluded / ndc_excluded.zip 0efc9e666f02…f202fb6c5f17…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 46 of 55 · 1,088 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Vichy Laboratoires Normaderm Daily Deep Cleansing Acne Treatment SALICYLIC ACID L'Oreal USA Products Inc 74c49388-3314-47e8-80b1-19c09e6ea1f9 2024-07-14 Warnings Exact identifier application number: M006 Vichy Laboratoires Normaderm Daily Deep Cleansing Acne Treatment SALICYLIC ACID COSMETIQUE ACTIVE PRODUCTION 873de079-8b8d-45cd-8c7c-4645818f5aaa 2024-07-14 Warnings Exact identifier application number: M006 Dr. Zenovia Clear Complexion SALICYLIC ACID Topiderm, Inc. 4ff9b26d-3cd9-4539-b389-edd2df24a466 2024-06-28 Warnings Exact identifier application number: M006 LEROSETT Botanical Acne Cleanser SALICYLIC ACID GUNILLA OF SWEDEN, INC. 8b31d155-c257-4452-9e22-0c69fa36173e 2024-06-27 Warnings Exact identifier application number: M006 SkinCeuticals Silymarin CF Acne Treatment Antioxidant SALICYLIC ACID Cosmetique Active Production fcc3c44b-3090-45b5-91e4-e591c92a08c8 2024-06-24 Warnings Exact identifier application number: M006 Peace Out Early Stage Acne Dot SALICYLIC ACID Peace Out LLC. 0632d458-d326-ade4-e063-6294a90af3ba 2024-06-20 Warnings Exact identifier application number: M006 Replenix BP Acne BENZOYL PEROXIDE Topiderm, Inc. f449e020-a4d8-4a1b-82eb-4dc59e99b8d4 2024-06-18 Warnings Exact identifier application number: M006 b pure Pressed Powder for Acne Prone Skin Fair SALICYLIC ACID Fourstar Group USA, Inc. ecf22bd1-4fc3-4455-ae01-13f97f53dc34 2024-06-17 Warnings Exact identifier application number: M006 b pure Pressed Powder for Acne Prone Skin Tan SALICYLIC ACID Fourstar Group USA, Inc. 1158f6c2-2b59-4ed3-8d28-73b6da885a5d 2024-06-17 Warnings Exact identifier application number: M006 Gly-Sal 10-2 SALICYLIC ACID Topiderm, Inc. 661cc58b-9360-4b96-b405-afdc2e378397 2024-06-13 Warnings Exact identifier application number: M006 BLAIR and JACK Anti-Bump Acne Treatment BENZOYL PEROXIDE Blair + Jack aa8df86a-639c-4416-aadf-4b58566ed9f1 2024-06-11 Warnings Exact identifier application number: M006 b pure Blemish Concealer for Acne Prone Skin Nude SALICYLIC ACID Fourstar Group USA, Inc. 76e91277-1fb4-490b-b351-39d626bc1fc2 2024-06-11 Warnings Exact identifier application number: M006 b pure Blemish Concealer for Acne Prone Skin Fair SALICYLIC ACID Fourstar Group USA, Inc. 764599e5-2ec3-4223-819e-36415fd915f7 2024-06-11 Warnings Exact identifier application number: M006 Dr. Zenovia Acne Cleanser BENZOYL PEROXIDE Topiderm, Inc. 00fb1ee5-6076-4980-8507-9e58a96e6a6b 2024-06-11 Warnings Exact identifier application number: M006 Dr. Zenovia Spot Treatment BENZOYL PEROXIDE Topiderm, Inc. dfdb3d8e-4d39-4ce4-851f-80b11972ca9e 2024-06-11 Warnings Exact identifier application number: M006 Rugby Benzoyl Peroxide Acne Medication BENZOYL PEROXIDE NuCare Pharmaceuticals,Inc. 69bd4f4c-017a-7422-e053-2991aa0aa655 2024-06-10 Warnings Exact identifier application number: M006 Thayers Natural Remedies Since 1847 Rapid Acne Treatment SULFUR L'Oreal USA Products Inc d7cc3c06-2f89-4c0b-b121-fdd53638b625 2024-06-07 Warnings Exact identifier application number: M006 Differin 10% BPO Acne Treatment BENZOYL PEROXIDE Galderma Laboratories, L.P. 05468eab-f239-42cb-9106-055a105f0fa5 2024-06-06 Warnings Exact identifier application number: M006 2.5 Acne Med BENZOYL PEROXIDE Face Reality, Inc. 58a7f677-996c-4951-8e5d-b5556244f800 2024-06-05 Warnings Exact identifier application number: M006 10 Acne Med BENZOYL PEROXIDE Face Reality, Inc. 91791905-086f-44cf-9c1a-e9f132c6c11b 2024-06-05 Warnings Exact identifier application number: M006
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