Lip Ice Coco Vanilla

Manufacturer: The Mentholatum Company
Effective date: 2018-08-08
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:56:43

Label at a glance#

ProductLip Ice Coco Vanilla

Active ingredientDIMETHICONE, OCTINOXATE, OCTISALATE

Label structure2 sections

Label contents#

Full prescribing information#

Package/Label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DailyMed Pharmacologic Classes#

Class, Version, Type table
Class	Version	Type	Effective
DIMETHICONE Pharmacologic Class Indexing	3	Indexing - Pharmacologic Class	20180813

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
10742-8877-1	Lip Ice Coco Vanilla	1 in 1 BLISTER PACK	LIPSTICK	1		1
10742-8877-1	Lip Ice Coco Vanilla	3.5 g in 1 CYLINDER	LIPSTICK	3.5		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
10742-8877	LIP ICE COCO VANILLA (DIMETHICONE, OCTINOXATE, OCTISALATE) LIPSTICK [THE MENTHOLATUM COMPANY]	1	2 package rows	20180901_de8dc95f-23f2-4f67-a652-c92966c1bd4b.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

Lip Ice Coco Vanilla
dimethicone, octinoxate, octisalate
DIMETHICONE
OCTINOXATE
OCTISALATE
MINERAL OIL
CERESIN
PETROLATUM
LANOLIN
CAMPHOR (SYNTHETIC)
MENTHOL, UNSPECIFIED FORM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
10742-8877	10742-8877-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
DIMETHICONE	92RU3N3Y1O	ACTIB
OCTINOXATE	4Y5P7MUD51	ACTIB
OCTISALATE	4X49Y0596W	ACTIB
MINERAL OIL	T5L8T28FGP	IACT
CERESIN	Q1LS2UJO3A	IACT
PETROLATUM	4T6H12BN9U	IACT
LANOLIN	7EV65EAW6H	IACT
CAMPHOR (SYNTHETIC)	5TJD82A1ET	IACT
MENTHOL, UNSPECIFIED FORM	L7T10EIP3A	IACT

Source Document#

Source XML · Source PDF

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
de8dc95f-23f2-4f67-a652-c92966c1bd4b			de8dc95f-23f2-4f67-a652-c92966c1bd4b	2018-08-08		Exact identifier spl id: de8dc95f-23f2-4f67-a652-c92966c1bd4b spl set id: de8dc95f-23f2-4f67-a652-c92966c1bd4b

Reported adverse events (FAERS/openFDA)#

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