acne and blemish control mask
Generic: sulfer
Labeler: usrx llcDrug Facts
Product Profile
Brand Name
acne and blemish control mask
Generic Name
sulfer
Labeler
usrx llc
Dosage Form
CREAM
Routes
Active Ingredients
sulfur 5 g/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
70809-1906
Product ID
70809-1906_236fe910-575e-8ef3-e063-6394a90a222e
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M006
Listing Expiration
2026-12-31
Marketing Start
2020-04-28
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
708091906
Hyphenated Format
70809-1906
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 and blemish control mask (source: ndc)
Generic Name
sulfer (source: ndc)
Application Number
M006 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 g/100mL
Packaging
- 1 TUBE in 1 BOX (70809-1906-1) / 73.93 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": "236fe910-575e-8ef3-e063-6394a90a222e", "openfda": {"unii": ["70FD1KFU70"], "rxcui": ["1291231"], "spl_set_id": ["a45c4f71-223b-169a-e053-2995a90acc86"], "manufacturer_name": ["USRX LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 BOX (70809-1906-1) / 73.93 mL in 1 TUBE", "package_ndc": "70809-1906-1", "marketing_start_date": "20200428"}], "brand_name": "ACNE AND BLEMISH CONTROL MASK", "product_id": "70809-1906_236fe910-575e-8ef3-e063-6394a90a222e", "dosage_form": "CREAM", "product_ndc": "70809-1906", "generic_name": "SULFER", "labeler_name": "USRX LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ACNE AND BLEMISH CONTROL MASK", "active_ingredients": [{"name": "SULFUR", "strength": "5 g/100mL"}], "application_number": "M006", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200428", "listing_expiration_date": "20261231"}