Home NDC 0299-3839-01 NDC 0299-3839-01 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 0299-3839
Requested NDC 0299-3839-01
Package NDCs from labels 0299-3839-01
Manufacturer National Council for Prescription Drug Programs
Effective date 2012-07-24
Current FDA listing Not matched in FDA.report NDC product tables 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 7 · 132 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join SULFUR CALMING MASK SULFUR CONTROL CORRECTIVE SKINCARE INC 446bd2ea-da88-422a-b086-e61b2d5b6269 2025-12-31 Warnings Name fallback generic name: SULFUR THYLOX SULFUR Bradford Soap Works, Inc. 5f52b769-9893-4391-b98f-3765e7b49485 2025-12-31 Warnings Name fallback generic name: SULFUR Spot Defy SULFUR Bioelements, Inc. 6f35f950-8d04-4181-a897-5679fde1e2d9 2025-12-17 Warnings Name fallback generic name: SULFUR Cetaphil Redness Relieving Daily Facial Moisturizer with sunscreen SPF 40 TITANIUM DIOXIDE, ZINC OXIDE Galderma Laboratories, L.P. 45d101be-2b88-4759-9ccc-556f5ec0553d 2025-12-17 Warnings Name fallback manufacturer name: Galderma Laboratories, L.P. DRx Blemish Clarifying Mask SULFUR Dr. Dennis Gross Skincare 7093a8d4-1910-4b23-9d88-d3398db0916a 2025-12-15 Warnings Name fallback generic name: SULFUR PowerSpot Cleanse SULFUR Bluemercury 443ae172-bacd-4122-8d78-d2214bcb02fd 2025-12-09 Warnings Name fallback generic name: SULFUR Dermaharmony 10% Sulfur SULFUR D3 Development, Inc. c78ead80-a8ee-0b52-e053-2a95a90ab880 2025-12-01 Warnings Name fallback generic name: SULFUR Dermaharmony 10% Sulfur with Tea Tree Oil SULFUR D3 Development, Inc. c79005d4-0c6f-75d0-e053-2995a90a8314 2025-12-01 Warnings Name fallback generic name: SULFUR EradiKate ACNE TREATMENT SULFUR Rare Beauty Brands Inc 44ebacf3-52c1-4896-e063-6394a90ac447 2025-12-01 Warnings Name fallback generic name: SULFUR EradiKate Daily Foaming Cleanser Acne Treatment SULFUR Rare Beauty Brands Inc. 44ebc725-796f-71e6-e063-6294a90a69a6 2025-12-01 Warnings Name fallback generic name: SULFUR Blemish Buster Solution Acne Treatment SULFUR Guthy-Renker LLC d2b9462d-7897-40a4-9022-eeb04e7d5adf 2025-12-01 Warnings Name fallback generic name: SULFUR Anna Guanche MD Miracle Cream The Pimple Cream SULFUR Bella Cosmeceuticals, Inc. b4562cf4-aae3-e9db-e053-2995a90a7210 2025-11-30 Warnings Name fallback generic name: SULFUR Ayadara Cystic Acne Spot Treatment SULFUR Leiluna LLC 3cc17e7a-34d4-4789-a387-40e4d781091b 2025-11-25 Warnings Name fallback generic name: SULFUR Cetaphil Soothing Gel Cream ALLANTOIN Galderma Laboratories, L.P. bab404f0-2f7a-4bac-b053-cbdc81c029b5 2025-11-24 Warnings Name fallback manufacturer name: Galderma Laboratories, L.P. Cetaphil Sun Tinted Face SPF 40 TITANIUM DIOXIDE, ZINC OXIDE Galderma Laboratories, L.P. 22413f93-7219-4726-b741-2392e576b34a 2025-11-24 Warnings Name fallback manufacturer name: Galderma Laboratories, L.P. Shaant Spot Hero Drying Acne Treatment SULFUR Codex Labs Corporation 24fa844b-e4ce-46de-a2d6-e9e863888a55 2025-11-21 Warnings Name fallback generic name: SULFUR Naturium Sulfur Spot Treatment 8% SULFUR e.l.f. Cosmetics, Inc 0a4a9aed-5eeb-f648-e063-6394a90a1d76 2025-11-14 Warnings Name fallback generic name: SULFUR Clinicians Complex SULFUR Cosmed Dermaceuticals, Inc. 256e3e4e-2219-45f8-ab78-a6a541767de8 2025-11-11 Warnings Name fallback generic name: SULFUR Clinicians Complex SULFUR SkinSx.com, Inc. 0f13770a-774b-49ad-8417-02928371682a 2025-11-11 Warnings Name fallback generic name: SULFUR SUPPORT SERUM FORTIFIED SULFUR ZENMED Raging Creations Ltd. 26e5777d-4ce2-458c-90f1-4c23c7b571ed 2025-11-10 Warnings Name fallback generic name: SULFUR
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.