BIOSILK POMEGRANITE- benzalkonium chloride lotion

Biosilk Pomegranite by

Drug Labeling and Warnings

Biosilk Pomegranite by is a Otc medication manufactured, distributed, or labeled by Farouk Systems, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Active ingredient Purpose
Benzalkonium Chloride 0.13%................................Antimicrobial

Warnings

Stop use and ask a doctor if irritation and redness develop

Warnings

Keep out of reach of children. In case of accidental ingestion,
get medical help or contact a Poison Control Center immediately.

Warnings

When using this product
avoid contact with eyes
if contact occurs, rinse eyes thoroughly with water

Warnings

Warnings
For external use only.
When using this product
avoid contact with eyes
if contact occurs, rinse eyes thoroughly with water
Stop use and ask a doctor if irritation and redness develop
Keep out of reach of children. In case of accidental ingestion,
get medical help or contact a Poison Control Center immediately.

Inactive Ingredients

Inactive ingredients: Aqua/Water/Eau, Cetyl Alcohol,
Dimethicone, Propanediol, Cetearyl Alcohol, C15-19 Alkane,
Glycerin, Glyceryl Stearate SE, Ceteareth-20, Caprylyl Glycol,
Aloe Barbadensis Leaf Juice, Hydrolyzed Silk, Hexylene
Glycol, Dimethiconol, Butyrospermum Parkii (Shea) Butter,
Pentylene Glycol, Ethylhexylglycerin, Disodium EDTA,
Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Sodium
Hydroxide, Alcohol Denat., Fragrance (Parfum), Citral,
Citronellol, Limonene, Linalool

Directions

apply a small amount to palm and rub hands together thoroughly

Use(s)

Use[s] to help reduce bacteria on the skin
recommended for routine use

Use(s)

Use[s] to help reduce bacteria on the skin

Biosilk

Biosilk

Health+Care

ANTIBACTERIAL
SHIELD
LOTION WITH ALOE VERA, POMEGRANATE

& SILK

95% Natural Paraben Free

KILLS 99.9% OF GERMS
FDA REGISTRATION #
NDC: 73740-5003-1
PARABEN FREE
pH ~5.5

MADE IN THE USA

12 FL OZ (355 mL)

INGREDIENTS AND APPEARANCE

BIOSILK POMEGRANITE 
benzalkonium chloride lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73740-5003
Route of Administration	CUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
DIMETHICONE 1000 (UNII: MCU2324216)	3.64 g  in 100 g
DIMETHICONOL (100000 CST) (UNII: OSA9UP217S)	0.36 g  in 100 g
EDETATE DISODIUM (UNII: 7FLD91C86K)	0.15 g  in 100 g
SILK, ENZYME HYDROLYZED (1000 MW) (UNII: 960MDR3Z07)	0.0011 g  in 100 g
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)	1.6 g  in 100 g
CAPRYLYL GLYCOL (UNII: 00YIU5438U)	1 g  in 100 g
FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF)	0.23538 g  in 100 g
LIMONENE, (+)- (UNII: GFD7C86Q1W)	0.05139 g  in 100 g
ALCOHOL (UNII: 3K9958V90M)	0.013 g  in 100 g
HEXYLENE GLYCOL (UNII: KEH0A3F75J)	0.4 g  in 100 g
BUTYROSPERMUM PARKII (SHEA) BUTTER UNSAPONIFIABLES (UNII: 0C9AC7D6XU)	0.3 g  in 100 g
PENTYLENE GLYCOL (UNII: 50C1307PZG)	0.3 g  in 100 g
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)	0.2 g  in 100 g
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)	0.1 g  in 100 g
CITRAL (UNII: T7EU0O9VPP)	0.00294 g  in 100 g
.BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)	0.00588 g  in 100 g
C15-19 ALKANE (UNII: CI87N1IM01)	2 g  in 100 g
GLYCERIN (UNII: PDC6A3C0OX)	2 g  in 100 g
POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)	1.6 g  in 100 g
LINALOOL, (+/-)- (UNII: D81QY6I88E)	0.00441 g  in 100 g
PROPANEDIOL (UNII: 5965N8W85T)	2.1 g  in 100 g
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)	2 g  in 100 g
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.001 g  in 100 g
SODIUM HYDROXIDE (UNII: 55X04QC32I)	0.02 g  in 100 g
WATER (UNII: 059QF0KO0R)	77.8849 g  in 100 g
CETYL ALCOHOL (UNII: 936JST6JCN)	3.9 g  in 100 g

Product Characteristics
Color		Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73740-5003-1	355 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	08/24/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		08/24/2020

Labeler - Farouk Systems, Inc. (137598132)

Registrant - Farouk Systems, Inc. (137598132)

Establishment
Name	Address	ID/FEI	Business Operations
Farouk Systems, Inc.		137598132	manufacture(73740-5003)