anti bacterial hand gel ghoul friend
Generic: alcohol
Labeler: bath & body works, inc.Drug Facts
Product Profile
Brand Name
anti bacterial hand gel ghoul friend
Generic Name
alcohol
Labeler
bath & body works, inc.
Dosage Form
GEL
Routes
Active Ingredients
alcohol 71 mL/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
62670-6843
Product ID
62670-6843_4c9c2080-0714-861c-e063-6394a90aa1b2
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2027-12-31
Marketing Start
2025-06-30
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
626706843
Hyphenated Format
62670-6843
Supplemental Identifiers
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
anti bacterial hand gel ghoul friend (source: ndc)
Generic Name
alcohol (source: ndc)
Application Number
505G(a)(3) (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 71 mL/100mL
Packaging
- 29 mL in 1 BOTTLE (62670-6843-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4c9c2080-0714-861c-e063-6394a90aa1b2", "openfda": {"unii": ["3K9958V90M"], "spl_set_id": ["38e20376-982f-80b8-e063-6394a90ab5f8"], "manufacturer_name": ["Bath & Body Works, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "29 mL in 1 BOTTLE (62670-6843-0)", "package_ndc": "62670-6843-0", "marketing_start_date": "20250630"}], "brand_name": "Anti Bacterial Hand Gel Ghoul Friend", "product_id": "62670-6843_4c9c2080-0714-861c-e063-6394a90aa1b2", "dosage_form": "GEL", "product_ndc": "62670-6843", "generic_name": "Alcohol", "labeler_name": "Bath & Body Works, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Anti Bacterial Hand Gel", "brand_name_suffix": "Ghoul Friend", "active_ingredients": [{"name": "ALCOHOL", "strength": "71 mL/100mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250630", "listing_expiration_date": "20271231"}