plus brasept alcocol gel
Generic: alcohol
Labeler: newdrop north america llcDrug Facts
Product Profile
Brand Name
plus brasept alcocol gel
Generic Name
alcohol
Labeler
newdrop north america llc
Dosage Form
GEL
Routes
Active Ingredients
alcohol .7 mL/mL
Manufacturer
Identifiers & Regulatory
Product NDC
83318-605
Product ID
83318-605_440c5ac8-dc18-6db4-e063-6294a90a6f19
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2023-03-24
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
83318605
Hyphenated Format
83318-605
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
plus brasept alcocol gel (source: ndc)
Generic Name
alcohol (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .7 mL/mL
Packaging
- 208200 mL in 1 DRUM (83318-605-08)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "440c5ac8-dc18-6db4-e063-6294a90a6f19", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["581662"], "spl_set_id": ["f791c99c-5879-9ba2-e053-6394a90ad3c7"], "manufacturer_name": ["NEWDROP NORTH AMERICA LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "208200 mL in 1 DRUM (83318-605-08)", "package_ndc": "83318-605-08", "marketing_start_date": "20240625"}], "brand_name": "Plus Brasept Alcocol Gel", "product_id": "83318-605_440c5ac8-dc18-6db4-e063-6294a90a6f19", "dosage_form": "GEL", "product_ndc": "83318-605", "generic_name": "ALCOHOL", "labeler_name": "NEWDROP NORTH AMERICA LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Plus Brasept Alcocol Gel", "active_ingredients": [{"name": "ALCOHOL", "strength": ".7 mL/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230324", "listing_expiration_date": "20261231"}