BIOSOLIS Face Sunscreen broad spectrum SPF30

Product NDC: 61296-018
Requested package NDC: 61296-018-00
11-digit product format: 612960018
Labeler code: 61296
Product ID: 61296-018_eff52842-7643-c4ec-e053-2995a90a6dc3
Type: HUMAN OTC DRUG
Nonproprietary name: ZINC OXIDE
Dosage form: CREAM
Route: TOPICAL
Labeler: Pro Vera SA
Application: part352
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2022-01-07
Marketing end: 0000-00-00
Substance: ZINC OXIDE
Active strength: 188 mg/mL
Pharmacologic classes: Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
NDC exclude flag: No
Listing certified through: 2023-12-31
Current FDA listing: Historical FDA.report record

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

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	61296-018	61296-018-00	D	Discontinued by firm		2026-07-31

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	Marketing start	Marketing end	Sample	Exclude flag	Status
61296-018-00	61296001800	1 BOTTLE, PUMP in 1 BOX (61296-018-00) > 50 mL in 1 BOTTLE, PUMP	2022-01-07	0000-00-00	No	No	Current