Baby Skin Mineral Sunscreen

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 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	79265-8578	79265-8578-3	D	Discontinued by firm		2026-10-05

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

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
6bd95106-a412-1dad-b9cc-4cb74bfb27ce	Product name	2	20230315
290f523a-f9db-9774-b5a9-e1f908ac1782	Product name	1	20150828
c6b65c52-69c7-df49-550a-a50c137f6218	Product name	1	20140508

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
79265-8578-3	Baby Skin Mineral Sunscreen	89 mL in 1 TUBE	LOTION	89		3

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
79265-8578	BABY SKIN MINERAL SUNSCREEN (MINERAL SUNSCREEN) LOTION [BABO BOTANICALS, INC.]	3	Legacy NDC, 1 package rows	20241215_b0a4ac6b-8f88-8a9a-e053-2995a90ab10e.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
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
79265-8578-3	79265857803	89 mL in 1 TUBE (79265-8578-3)	89 ml	2020-08-26	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
8578 SPF 50 Baby Skin Mineral Sunscreen Lotion	Babo Botanicals, Inc. \| Bell International Laboratories	2024-12-12	HUMAN OTC DRUG LABEL	3