naturium sulfur spot treatment 8%
Generic: sulfur
Labeler: e.l.f. cosmetics, incDrug Facts
Product Profile
Brand Name
naturium sulfur spot treatment 8%
Generic Name
sulfur
Labeler
e.l.f. cosmetics, inc
Dosage Form
LIQUID
Routes
Active Ingredients
sulfur 80 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
76354-120
Product ID
76354-120_43961b71-929a-943b-e063-6294a90afd73
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M006
Listing Expiration
2026-12-31
Marketing Start
2022-06-17
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
76354120
Hyphenated Format
76354-120
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
naturium sulfur spot treatment 8% (source: ndc)
Generic Name
sulfur (source: ndc)
Application Number
M006 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 80 mg/mL
Packaging
- 1 TUBE in 1 CARTON (76354-120-01) / 15 mL in 1 TUBE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "43961b71-929a-943b-e063-6294a90afd73", "openfda": {"unii": ["70FD1KFU70"], "rxcui": ["2605592"], "spl_set_id": ["0a4a9aed-5eeb-f648-e063-6394a90a1d76"], "manufacturer_name": ["e.l.f. Cosmetics, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (76354-120-01) / 15 mL in 1 TUBE", "package_ndc": "76354-120-01", "marketing_start_date": "20220617"}], "brand_name": "Naturium Sulfur Spot Treatment 8%", "product_id": "76354-120_43961b71-929a-943b-e063-6294a90afd73", "dosage_form": "LIQUID", "product_ndc": "76354-120", "generic_name": "Sulfur", "labeler_name": "e.l.f. Cosmetics, Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Naturium Sulfur Spot Treatment 8%", "active_ingredients": [{"name": "SULFUR", "strength": "80 mg/mL"}], "application_number": "M006", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220617", "listing_expiration_date": "20261231"}