dr lift mineral spf 30
Generic: titanium dioxide
Labeler: spa de soleilDrug Facts
Product Profile
Brand Name
dr lift mineral spf 30
Generic Name
titanium dioxide
Labeler
spa de soleil
Dosage Form
SPRAY
Routes
Active Ingredients
titanium dioxide 72 mg/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
68062-8312
Product ID
68062-8312_40c0e413-70f6-25c9-e063-6294a90ad27d
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M020
Listing Expiration
2026-12-31
Marketing Start
2025-10-09
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
680628312
Hyphenated Format
68062-8312
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
dr lift mineral spf 30 (source: ndc)
Generic Name
titanium dioxide (source: ndc)
Application Number
M020 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 72 mg/100mL
Packaging
- 100 mL in 1 BOTTLE, SPRAY (68062-8312-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "40c0e413-70f6-25c9-e063-6294a90ad27d", "openfda": {"unii": ["15FIX9V2JP"], "spl_set_id": ["40c0e0d2-2c1d-e629-e063-6394a90a5aaf"], "manufacturer_name": ["Spa de Soleil"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE, SPRAY (68062-8312-1)", "package_ndc": "68062-8312-1", "marketing_start_date": "20251009"}], "brand_name": "Dr Lift Mineral SPF 30", "product_id": "68062-8312_40c0e413-70f6-25c9-e063-6294a90ad27d", "dosage_form": "SPRAY", "product_ndc": "68062-8312", "generic_name": "titanium dioxide", "labeler_name": "Spa de Soleil", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Dr Lift Mineral SPF 30", "active_ingredients": [{"name": "TITANIUM DIOXIDE", "strength": "72 mg/100mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20251009", "listing_expiration_date": "20261231"}