acne lotionsulfur sulfur
Generic: sulfur
Labeler: allure labs incDrug Facts
Product Profile
Brand Name
acne lotionsulfur sulfur
Generic Name
sulfur
Labeler
allure labs inc
Dosage Form
LOTION
Routes
Active Ingredients
sulfur 30 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
62742-4169
Product ID
62742-4169_b392c601-8a30-414a-a63c-517c08537e0a
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH FINAL
Application Number
part333D
Listing Expiration
2026-12-31
Marketing Start
2018-11-09
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
627424169
Hyphenated Format
62742-4169
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
acne lotionsulfur sulfur (source: ndc)
Generic Name
sulfur (source: ndc)
Application Number
part333D (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 30 mg/mL
Packaging
- 55 mL in 1 BOTTLE, PUMP (62742-4169-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "b392c601-8a30-414a-a63c-517c08537e0a", "openfda": {"unii": ["70FD1KFU70"], "rxcui": ["245607"], "spl_set_id": ["487d2e65-7fb0-4eee-a082-6b2c192eaf27"], "manufacturer_name": ["Allure Labs Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "55 mL in 1 BOTTLE, PUMP (62742-4169-1)", "package_ndc": "62742-4169-1", "marketing_start_date": "20181109"}], "brand_name": "Acne LotionSulfur Sulfur", "product_id": "62742-4169_b392c601-8a30-414a-a63c-517c08537e0a", "dosage_form": "LOTION", "product_ndc": "62742-4169", "generic_name": "Sulfur", "labeler_name": "Allure Labs Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acne LotionSulfur", "brand_name_suffix": "Sulfur", "active_ingredients": [{"name": "SULFUR", "strength": "30 mg/mL"}], "application_number": "part333D", "marketing_category": "OTC MONOGRAPH FINAL", "marketing_start_date": "20181109", "listing_expiration_date": "20261231"}