Label: BIOSILK POMEGRANITE- benzalkonium chloride lotion
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Contains inactivated NDC Code(s)
NDC Code(s): 73740-5003-1 - Packager: Farouk Systems, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated August 24, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Warnings
- Warnings
- Warnings
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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.
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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
- Use(s)
- Use(s)
- Biosilk
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INGREDIENTS AND APPEARANCE
BIOSILK POMEGRANITE
benzalkonium chloride lotionProduct 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)