avant 70% alcohol gel
Generic: alcohol
Labeler: b4 ventures llcDrug Facts
Product Profile
Brand Name
avant 70% alcohol gel
Generic Name
alcohol
Labeler
b4 ventures llc
Dosage Form
GEL
Routes
Active Ingredients
alcohol 70 mL/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
68306-116
Product ID
68306-116_0a9bb5e2-3bbe-c534-e063-6394a90ac288
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2023-01-12
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68306116
Hyphenated Format
68306-116
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
avant 70% alcohol gel (source: ndc)
Generic Name
alcohol (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 70 mL/100mL
Packaging
- 208198 mL in 1 DRUM (68306-116-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "0a9bb5e2-3bbe-c534-e063-6394a90ac288", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["581662"], "spl_set_id": ["241f4334-2e88-4f7b-a0c7-c93da9f5086c"], "manufacturer_name": ["B4 Ventures LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "208198 mL in 1 DRUM (68306-116-01)", "package_ndc": "68306-116-01", "marketing_start_date": "20230112"}], "brand_name": "Avant 70% Alcohol Gel", "product_id": "68306-116_0a9bb5e2-3bbe-c534-e063-6394a90ac288", "dosage_form": "GEL", "product_ndc": "68306-116", "generic_name": "Alcohol", "labeler_name": "B4 Ventures LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Avant 70% Alcohol Gel", "active_ingredients": [{"name": "ALCOHOL", "strength": "70 mL/100mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230112", "listing_expiration_date": "20261231"}