dr. c. tuna sun bronzing oil spf 6
Generic: octinoxate
Labeler: farmasi us llcDrug Facts
Product Profile
Brand Name
dr. c. tuna sun bronzing oil spf 6
Generic Name
octinoxate
Labeler
farmasi us llc
Dosage Form
OIL
Routes
Active Ingredients
octinoxate 35 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
74690-014
Product ID
74690-014_09735fbf-7779-ca3f-e063-6294a90a9f94
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M020
Listing Expiration
2026-12-31
Marketing Start
2021-07-25
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
74690014
Hyphenated Format
74690-014
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. c. tuna sun bronzing oil spf 6 (source: ndc)
Generic Name
octinoxate (source: ndc)
Application Number
M020 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 35 mg/mL
Packaging
- 1 BOTTLE in 1 BOX (74690-014-01) / 115 mL in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "09735fbf-7779-ca3f-e063-6294a90a9f94", "openfda": {"unii": ["4Y5P7MUD51"], "spl_set_id": ["91b428cc-1c80-4d56-8450-790c66de4133"], "manufacturer_name": ["Farmasi US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 BOX (74690-014-01) / 115 mL in 1 BOTTLE", "package_ndc": "74690-014-01", "marketing_start_date": "20210725"}], "brand_name": "Dr. C. Tuna Sun Bronzing Oil SPF 6", "product_id": "74690-014_09735fbf-7779-ca3f-e063-6294a90a9f94", "dosage_form": "OIL", "product_ndc": "74690-014", "generic_name": "OCTINOXATE", "labeler_name": "Farmasi US LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Dr. C. Tuna Sun Bronzing Oil SPF 6", "active_ingredients": [{"name": "OCTINOXATE", "strength": "35 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210725", "listing_expiration_date": "20261231"}