Tinted Mineral Sunscreen Broad Spectrum SPF 30

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded product	product	82418-0650		I	Inactivated by FDA		2026-10-05
excluded package	package	82418-0650	82418-0650-2	I	Inactivated by FDA		2026-10-05

Adverse event summaries are temporarily unavailable. Other product information remains available.

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
82418-0650-2	Tinted Mineral Sunscreen Broad Spectrum SPF 30	50 mL in 1 BOTTLE, PUMP	CREAM	50		2

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
82418-0650	TINTED MINERAL SUNSCREEN BROAD SPECTRUM SPF 30 (TITANIUM DIOXIDE AND ZINC OXIDE) CREAM [LOVE MEDICAL SPA LLC]	2	Legacy NDC, 1 package rows	20240117_ea37df9b-7eea-0477-e053-2995a90aab65.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
15FIX9V2JP	TITANIUM DIOXIDE	13463-67-7	TITANIUM DIOXIDE
SOI2LOH54Z	ZINC OXIDE	1314-13-2	ZINC OXIDE

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
82418-0650-2	82418065002	50 mL in 1 BOTTLE, PUMP (82418-0650-2)	50 ml	2022-08-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Tinted Mineral Sunscreen Broad Spectrum SPF 30	Love Medical Spa LLC	2024-01-16	HUMAN OTC DRUG LABEL	2