fineapple hand sanitizer
Generic: alcohol
Labeler: crop beauty group inc.Drug Facts
Product Profile
Brand Name
fineapple hand sanitizer
Generic Name
alcohol
Labeler
crop beauty group inc.
Dosage Form
GEL
Routes
Active Ingredients
alcohol .62 mL/mL
Manufacturer
Identifiers & Regulatory
Product NDC
78768-002
Product ID
78768-002_0897ccca-fa1b-873f-e063-6394a90a59ab
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
505G(a)(3)
Listing Expiration
2026-12-31
Marketing Start
2020-06-07
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
78768002
Hyphenated Format
78768-002
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
fineapple hand sanitizer (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 TUBE (78768-002-30)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "0897ccca-fa1b-873f-e063-6394a90a59ab", "openfda": {"unii": ["3K9958V90M"], "rxcui": ["581660"], "spl_set_id": ["316625c6-dd73-485c-a617-ed86ebf2ac02"], "manufacturer_name": ["CROP BEAUTY GROUP INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 mL in 1 TUBE (78768-002-30)", "package_ndc": "78768-002-30", "marketing_start_date": "20200607"}], "brand_name": "FINEAPPLE Hand Sanitizer", "product_id": "78768-002_0897ccca-fa1b-873f-e063-6394a90a59ab", "dosage_form": "GEL", "product_ndc": "78768-002", "generic_name": "ALCOHOL", "labeler_name": "CROP BEAUTY GROUP INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "FINEAPPLE Hand Sanitizer", "active_ingredients": [{"name": "ALCOHOL", "strength": ".62 mL/mL"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200607", "listing_expiration_date": "20261231"}