hanchobit sunscreen
Generic: titanium dioxide
Labeler: hanchoyeanbiotec co.,ltd.Drug Facts
Product Profile
Brand Name
hanchobit sunscreen
Generic Name
titanium dioxide
Labeler
hanchoyeanbiotec co.,ltd.
Dosage Form
CREAM
Routes
Active Ingredients
betula alba juice .01 mg/50mg
Manufacturer
Identifiers & Regulatory
Product NDC
85164-005
Product ID
85164-005_449ff8f8-fe08-7bce-e063-6394a90ace56
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M020
Listing Expiration
2026-12-31
Marketing Start
2025-11-07
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
85164005
Hyphenated Format
85164-005
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
hanchobit sunscreen (source: ndc)
Generic Name
titanium dioxide (source: ndc)
Application Number
M020 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .01 mg/50mg
Packaging
- 50 mg in 1 BOTTLE, PLASTIC (85164-005-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "449ff8f8-fe08-7bce-e063-6394a90ace56", "openfda": {"unii": ["9G931M6I4G"], "spl_set_id": ["42fd5d3e-4e98-86d7-e063-6294a90a45c2"], "manufacturer_name": ["HANCHOYEANBIOTEC Co.,Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 mg in 1 BOTTLE, PLASTIC (85164-005-01)", "package_ndc": "85164-005-01", "marketing_start_date": "20251107"}], "brand_name": "HANCHOBIT Sunscreen", "product_id": "85164-005_449ff8f8-fe08-7bce-e063-6394a90ace56", "dosage_form": "CREAM", "product_ndc": "85164-005", "generic_name": "TITANIUM DIOXIDE", "labeler_name": "HANCHOYEANBIOTEC Co.,Ltd.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "HANCHOBIT Sunscreen", "active_ingredients": [{"name": "BETULA ALBA JUICE", "strength": ".01 mg/50mg"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20251107", "listing_expiration_date": "20261231"}