Botao Kids Mineral Foam

Product NDC: 69435-1502
11-digit product format: 694351502
Labeler code: 69435
Product ID: 69435-1502_e145bf63-3f27-3247-e053-2995a90afab8
Type: HUMAN OTC DRUG
Nonproprietary name: ZINC OXIDE
Dosage form: LOTION
Route: TOPICAL
Labeler: Peer Pharm Ltd.
Application: part352
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2022-05-19
Marketing end: 0000-00-00
Substance: ZINC OXIDE
Active strength: 24 g/96g
NDC exclude flag: No
Listing certified through: 2023-12-31
Current FDA listing: Historical FDA.report record

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	69435-1502		D	Discontinued by firm		2026-10-05
excluded package	package	69435-1502	69435-1502-1	D	Discontinued by firm		2026-10-05

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 4 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	69435-1502-1	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	69435-1502-1	`f5e01cc5f278…`	`a2eaf40c39c3…`

Reported adverse events (FAERS/openFDA)#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
69435-1502-1	2024-02-19	C162847	48780-1	1030e365-0cfe-111a-e063-dadaa90a10e2	Botao Kids Mineral Foam Spray SPF 50 - 1
69435-1502-1	2024-01-30	C162847	48780-1	1030e365-0cfe-111a-e063-dadaa90a10e2	Botao Kids Mineral Foam Spray SPF 50 - 1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69435-1502	BOTAO KIDS MINERAL FOAM (ZINC OXIDE) LOTION [PEER PHARM LTD.]	2	Legacy NDC	20240220_e145bf58-23a1-955d-e053-2a95a90a071c.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
SOI2LOH54Z	ZINC OXIDE	1314-13-2	ZINC OXIDE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
69435-1502-1	69435150201	96 g in 1 BOTTLE, SPRAY (69435-1502-1)	96 g	2022-05-19	0000-00-00	No	No	Current