TREATMENT LIPSHINE

Manufacturer: BOBBI BROWN PROFESSIONAL COSMETICS INC | ESTEE LAUDER COSMETICS, LTD | ESTEE LAUDER N.V. | Len-Ron Manufacturing Division of Aramis Inc. | Aramis Inc. | Northtec Bristol | Northtec Keystone | PADC 1 | Estee Lauder Pennsylvania Distribution Center 2 | Estee Lauder Cosmetics, Ltd. | Estee Lauder Cosmetics Distribution Center | Estee Lauder Kabushiki Kaisha | Whitman Laboratories Ltd. | Aveda Corporation | MANA PRODUCTS INC
Effective date: 2010-05-13
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:24:31

Label at a glance#

ProductTREATMENT LIPSHINE SPF 15

Active ingredientOCTINOXATE

Label structure3 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENT: TITANIUM DIOXIDE 7.0%

WARNINGS SECTION

WARNING: STOP USE IF IRRITATION OCCURS

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL:

BOBBI BROWN

TREATMENT LIPSHINE SPF 15

NET WT/POIDS NET 0.7 OZ./2 g

BOBBI BROWN PROFESSIONAL COSMETICS INC.

NEW YORK, NY 10022

FOLDING CARTON

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
64141-004-01	2020-01-31	C162847	48780-1	9d75b9d0-a5cd-f424-e053-dadaa90a57ce	8e5db199-4e6e-4a63-a84d-3a739ca99e7f

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
64141-004-01	TREATMENT LIPSHINESPF 15	1 in 1 CARTON	LIPSTICK	1		1
64141-004-02	TREATMENT LIPSHINESPF 15	2 g in 1 CARTRIDGE	LIPSTICK	2		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
64141-004	TREATMENT LIPSHINE SPF 15 (OCTINOXATE) LIPSTICK [BOBBI BROWN PROFESSIONAL COSMETICS INC]	1	Legacy NDC, 2 package rows	20100514_8e5db199-4e6e-4a63-a84d-3a739ca99e7f.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version	Uploaded
OCTINOXATE	ACTIVE INGREDIENT	4Y5P7MUD51	1
OCTINOXATE	ACTIVE MOIETY	4Y5P7MUD51	1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 2 matching rows.

TREATMENT LIPSHINE SPF 15
OCTINOXATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
64141-004	64141-004-02, 64141-004-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
OCTINOXATE	4Y5P7MUD51	ACTIB

Source Document#

Source XML

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
14f94091-c417-4a69-b622-ef9aa412e9e4			8e5db199-4e6e-4a63-a84d-3a739ca99e7f	2010-05-13	Warnings	Exact identifier spl id: 14f94091-c417-4a69-b622-ef9aa412e9e4 spl set id: 8e5db199-4e6e-4a63-a84d-3a739ca99e7f

Reported adverse events (FAERS/openFDA)#

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