peppermint hand sanitizer boy
Generic: alcohol
Labeler: k7 design group inc.Drug Facts
Product Profile
Brand Name
peppermint hand sanitizer boy
Generic Name
alcohol
Labeler
k7 design group inc.
Dosage Form
GEL
Routes
Active Ingredients
alcohol .62 mL/mL
Manufacturer
Identifiers & Regulatory
Product NDC
74177-010
Product ID
74177-010_08968b1b-1541-480e-e063-6294a90a5414
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2020-05-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
74177010
Hyphenated Format
74177-010
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
peppermint hand sanitizer boy (source: ndc)
Generic Name
alcohol (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .62 mL/mL
Packaging
- 30 mL in 1 BOTTLE (74177-010-30)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "08968b1b-1541-480e-e063-6294a90a5414", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["581660"], "spl_set_id": ["94ac4174-532a-4944-aa49-67060787e6a1"], "manufacturer_name": ["K7 Design Group Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 mL in 1 BOTTLE (74177-010-30)", "package_ndc": "74177-010-30", "marketing_start_date": "20200501"}], "brand_name": "PEPPERMINT HAND SANITIZER boy", "product_id": "74177-010_08968b1b-1541-480e-e063-6294a90a5414", "dosage_form": "GEL", "product_ndc": "74177-010", "generic_name": "ALCOHOL", "labeler_name": "K7 Design Group Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "PEPPERMINT HAND SANITIZER boy", "active_ingredients": [{"name": "ALCOHOL", "strength": ".62 mL/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200501", "listing_expiration_date": "20261231"}