end-zit
Generic: sulfur
Labeler: abbe laboratories, inc.Drug Facts
Product Profile
Brand Name
end-zit
Generic Name
sulfur
Labeler
abbe laboratories, inc.
Dosage Form
LOTION, AUGMENTED
Routes
Active Ingredients
sulfur .05 g/mL
Manufacturer
Identifiers & Regulatory
Product NDC
68605-2001
Product ID
68605-2001_9a07e62f-1c38-4055-b5ae-b1c06d08dd69
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M006
Listing Expiration
2027-12-31
Marketing Start
2004-04-20
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
686052001
Hyphenated Format
68605-2001
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
end-zit (source: ndc)
Generic Name
sulfur (source: ndc)
Application Number
M006 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .05 g/mL
Packaging
- 14.78 mL in 1 BOTTLE, GLASS (68605-2001-2)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "9a07e62f-1c38-4055-b5ae-b1c06d08dd69", "openfda": {"unii": ["70FD1KFU70"], "rxcui": ["422938", "1094323"], "spl_set_id": ["afed5e8e-324c-44c6-abf6-72938376a4b2"], "manufacturer_name": ["ABBE Laboratories, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "14.78 mL in 1 BOTTLE, GLASS (68605-2001-2)", "package_ndc": "68605-2001-2", "marketing_start_date": "20040420"}], "brand_name": "END-ZIT", "product_id": "68605-2001_9a07e62f-1c38-4055-b5ae-b1c06d08dd69", "dosage_form": "LOTION, AUGMENTED", "product_ndc": "68605-2001", "generic_name": "SULFUR", "labeler_name": "ABBE Laboratories, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "END-ZIT", "active_ingredients": [{"name": "SULFUR", "strength": ".05 g/mL"}], "application_number": "M006", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20040420", "listing_expiration_date": "20271231"}