Teint Miracle Octinoxate Sunscreen Broad Spectrum SPF 15

Product NDC: 70581-004
11-digit product format: 705810004
Labeler code: 70581
Product ID: 70581-004_9aefcc19-0037-5be7-e053-2a95a90a17e6
Type: HUMAN OTC DRUG
Nonproprietary name: OCTINOXATE
Dosage form: CREAM
Route: TOPICAL
Labeler: BPS 60
Application: part352
Marketing category: OTC MONOGRAPH NOT FINAL
Marketing start: 2016-04-06
Marketing end: 0000-00-00
Substance: OCTINOXATE
Active strength: 30 mg/mL
NDC exclude flag: No
Listing certified through: 2020-12-31
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	70581-004		D	Discontinued by firm		2026-10-05
excluded package	package	70581-004	70581-004-01	D	Discontinued by firm		2026-10-05

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product: Yes
Brand name base: Teint Miracle Octinoxate Sunscreen Broad Spectrum SPF 15
Listing expiration: 2026-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
OCTINOXATE	30 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
4Y5P7MUD51	Internal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
9af44d18-d9b4-48eb-8484-a3b84b7bd115	Available on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70581-004-01	Teint Miracle Octinoxate Sunscreen Broad Spectrum SPF 15	1 in 1 BOX	CREAM	1		8
70581-004-01	Teint Miracle Octinoxate Sunscreen Broad Spectrum SPF 15	110 mL in 1 BOTTLE	CREAM	110		8

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70581-004	TEINT MIRACLE OCTINOXATE SUNSCREEN BROAD SPECTRUM SPF 15 (OCTINOXATE) CREAM [BPS 60]	8	Legacy NDC, 2 package rows	20231210_9af44d18-d9b4-48eb-8484-a3b84b7bd115.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Teint Miracle Octinoxate Sunscreen Broad Spectrum SPF 15	OCTINOXATE	BPS 60	9af44d18-d9b4-48eb-8484-a3b84b7bd115	2023-12-09	Warnings	Exact identifier ndc (product): 70581-004

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
4Y5P7MUD51	OCTINOXATE	83834-59-7	OCTINOXATE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
70581-004-01	70581000401	1 BOTTLE in 1 BOX (70581-004-01) > 110 mL in 1 BOTTLE	1 bottle	2016-04-06	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Teint Miracle Octinoxate Sunscreen Broad Spectrum SPF 15	BPS 60 \| SICOS ET CIE	2023-12-09	HUMAN OTC DRUG LABEL	8