Kinfield Sunglow Luminizing Sunscreen SPF 30

Product NDC: 81750-030
11-digit product format: 817500030
Labeler code: 81750
Product ID: 81750-030_f1e9261e-20e6-c1bc-e053-2a95a90ac1a6
Type: HUMAN OTC DRUG
Nonproprietary name: Kinfield Sunglow Luminizing Sunscreen SPF 30
Dosage form: LOTION
Route: TOPICAL
Labeler: Kinfield, Inc.
Application: part352
Marketing category: OTC MONOGRAPH FINAL
Marketing start: 2021-04-05
Marketing end: 0000-00-00
Substance: ZINC OXIDE
Active strength: 20 g/100g
Pharmacologic classes: Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE]
NDC exclude flag: No
Listing certified through: 2024-12-31
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	81750-030		D	Discontinued by firm		2026-10-12
excluded package	package	81750-030	81750-030-60	D	Discontinued by firm		2026-10-12

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 · 6 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Code	Status	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	81750-030-60	D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		I	Inactivated by FDA	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	81750-030-60	I	Inactivated by FDA	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		I	Inactivated by FDA	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	81750-030-60	I	Inactivated by FDA	`367a005e9d99…`	`383a685ebd0f…`

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
81750-030-60	2024-07-30	C162847	48780-1	1030e365-657c-111a-e063-dadaa90a10e2	DRUG FACTS
81750-030-60	2024-01-30	C162847	48780-1	1030e365-657c-111a-e063-dadaa90a10e2	DRUG FACTS

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
81750-030	KINFIELD SUNGLOW LUMINIZING SUNSCREEN SPF 30 LOTION [KINFIELD, INC.]	5	Legacy NDC	20241222_346409ee-ae61-463c-aea3-048b82cd9927.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
81750-030-60	81750003060	1 TUBE in 1 PACKAGE (81750-030-60) > 60 g in 1 TUBE	1 tube	2021-06-14	0000-00-00	No	No	Current