bella blu skin care non tinted sunscreen
Generic: zinc oxide
Labeler: bella blu studios incDrug Facts
Product Profile
Brand Name
bella blu skin care non tinted sunscreen
Generic Name
zinc oxide
Labeler
bella blu studios inc
Dosage Form
CREAM
Routes
Active Ingredients
zinc oxide 200 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
87099-205
Product ID
87099-205_4627bba6-90cc-1ee0-e063-6394a90a5df6
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M020
Listing Expiration
2026-12-31
Marketing Start
2022-08-31
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
87099205
Hyphenated Format
87099-205
Supplemental Identifiers
UNII
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
bella blu skin care non tinted sunscreen (source: ndc)
Generic Name
zinc oxide (source: ndc)
Application Number
M020 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 mg/g
Packaging
- 1.5 g in 1 PACKET (87099-205-15)
Packages (1)
Ingredients (1)
Linked Drug Pages (2)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4627bba6-90cc-1ee0-e063-6394a90a5df6", "openfda": {"unii": ["SOI2LOH54Z"], "spl_set_id": ["3f67134c-88e8-8513-e063-6294a90aaf5a"], "manufacturer_name": ["BELLA BLU STUDIOS INC"]}, "finished": true, "packaging": [{"sample": true, "description": "1.5 g in 1 PACKET (87099-205-15)", "package_ndc": "87099-205-15", "marketing_start_date": "20220831"}], "brand_name": "Bella Blu Skin Care Non Tinted Sunscreen", "product_id": "87099-205_4627bba6-90cc-1ee0-e063-6394a90a5df6", "dosage_form": "CREAM", "product_ndc": "87099-205", "generic_name": "Zinc Oxide", "labeler_name": "BELLA BLU STUDIOS INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Bella Blu Skin Care Non Tinted Sunscreen", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "200 mg/g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220831", "listing_expiration_date": "20261231"}