superSHOCK

Manufacturer: Avon Products, Inc.
Effective date: 2011-04-19
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:27:49

Label at a glance#

ProductsuperSHOCK Liquid Lip Shine

Active ingredientOCTINOXATE, OXYBENZONE

Label structure6 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS: Apply liberally before sun exposure.
Reapply as needed for SPF protection.

WARNINGS SECTION

WARNING: Discontinue
use if skin irritation develops or increases. If irritation
persists, consult a health care practitioner.

INDICATIONS & USAGE SECTION

USES: Helps prevent sunburn. Higher SPF gives
more sunburn protection.

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS/INGRÉDIENTS ACTIFS :
OCTINOXATE 5.00%, OXYBENZONE 3.00%.

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS/ INGRÉDIENTS
INACTIFS : POLYBUTENE, DIISOSTEARYL
FUMARATE, LANOLIN, SIMMONDSIA CHINENSIS
(JOJOBA) SEED OIL, DIISOSTEARYL
MALATE, PETROLATUM, MICROCRYSTALLINE
WAX/CIRE MICROCRISTALLINE, BARIUM
SULFATE, CALCIUM SODIUM BOROSILICATE,
SILICA, ETHYLENE/PROPYLENE/STYRENE
COPOLYMER, ISOPROPYL ISOSTEARATE, CALCIUM
ALUMINUM BOROSILICATE, OZOKERITE,
EUPHORBIA CERIFERA (CANDELILLA) WAX/CIRE
DE CANDELILLA, TOCOPHERYL ACETATE,
BUTYLENE/ETHYLENE/STYRENE COPOLYMER,
PARFUM/FRAGRANCE, TIN OXIDE, LECITHIN,
C12-15 ALKYL BENZOATE, ISOPROPYL TITANIUM
TRIISOSTEARATE, RETINYL PALMITATE,
ASCORBYL PALMITATE, BETA-CAROTENE. MAY
CONTAIN/PEUT CONTENIR : MICA/CI 77019,
TITANIUM DIOXIDE/CI 77891, RED 33 LAKE/CI
17200, RED 7 LAKE, IRON OXIDES, RED 7/CI
15850, RED 28 LAKE/CI 45410, YELLOW 5
LAKE/CI 19140, RED 6/CI 15850, RED 6 LAKE,
YELLOW 6 LAKE/CI 15985, CARMINE/CI 75470,
BLUE 1 LAKE/CI 42090, RED 21 LAKE, RED 21,
RED 22 LAKE, RED 27 LAKE, RED 40, YELLOW
10 LAKE, ORANGE 5, ORANGE 5 LAKE, BISMUTH
OXYCHLORIDE.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of PDPimage of label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
10096-0258-1	2019-10-29	C162847	48780-1	960f7f55-c746-8e05-e053-dbdaa90a074a	a8c2510c-75f5-4ef2-ac22-cc1358dbfbcf

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
10096-0258-1	superSHOCKLiquid Lip Shine	10.5 g in 1 VIAL	LIPSTICK	10.5		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
10096-0258	SUPERSHOCK LIQUID LIP SHINE (OCTINOXATE, OXYBENZONE) LIPSTICK [AVON PRODUCTS, INC.]	1	Legacy NDC, 1 package rows	20110422_a8c2510c-75f5-4ef2-ac22-cc1358dbfbcf.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
OCTINOXATE	ACTIVE INGREDIENT	4Y5P7MUD51	1
OXYBENZONE	ACTIVE INGREDIENT	95OOS7VE0Y	1
OCTINOXATE	ACTIVE MOIETY	4Y5P7MUD51	1
OXYBENZONE	ACTIVE MOIETY	95OOS7VE0Y	1

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

superSHOCK Liquid Lip Shine
OCTINOXATE, OXYBENZONE
OCTINOXATE
OXYBENZONE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
10096-0258	10096-0258-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
OCTINOXATE	4Y5P7MUD51	ACTIB
OXYBENZONE	95OOS7VE0Y	ACTIB

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
51a7f2c0-fea0-4432-92a4-717f8e9750cb			a8c2510c-75f5-4ef2-ac22-cc1358dbfbcf	2011-04-19	Warnings	Exact identifier spl id: 51a7f2c0-fea0-4432-92a4-717f8e9750cb spl set id: a8c2510c-75f5-4ef2-ac22-cc1358dbfbcf

Reported adverse events (FAERS/openFDA)#

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