AMERISILK by SHIELD LINE LLC AMERISILK- bzk shampoo

AMERISILK by

Drug Labeling and Warnings

AMERISILK by is a Otc medication manufactured, distributed, or labeled by SHIELD LINE LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Benzalkonium Chloride...0.10% w/w

Purpose

Antibacterial

Uses

for hand washing to decrease bacteria on the skin recommended for repeated use
for body wash to help reduce bacteria that can potentially cause disease

Warnings

​ For external use only

When using this product

Avoid contact with eyes, in case of eye contact flush with water

Stop use and ask a doctor

if irritation and redness develops

Keep out of reach of children

If swallowed, get medical help or Poison Control Center right away

Directions

Apply to hands and wet as needed, vigorously
work into a lather and rinse thoroughly

Other information

Store in a cool dry place below 104 F°

Inactive Ingredients:

Water, Sodium Laureth
Sulfate, CAPB, Polyquaternium 7, Sodium
Chloride, Cocamide MEA, Sodium C14-15 Olefin
Sulfonate, Sodium Benzoate, PEG-7 Glyceryl
Cocoate, Fragrance, Methylchloroisothiazolinone
and Methylisothiazolinone, Aloe Barbadensis Gel,
Disodium EDTA, Citric Acid, D&C RED # 33,
FD&C BLUE # 1

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

AMERISILK 
bzk shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52410-8042
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
COCAMIDE MEA (UNII: C80684146D)
SODIUM BENZOATE (UNII: OJ245FE5EU)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
D&C RED NO. 33 (UNII: 9DBA0SBB0L)
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
CITRIC ACID (UNII: 2968PHW8QP)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
EDETATE DISODIUM (UNII: 7FLD91C86K)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
POLYQUATERNIUM-7 (UNII: 0L414VCS5Y)
PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52410-8042-6	237 g in 1 BOTTLE; Type 0: Not a Combination Product	11/19/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	11/19/2025

Labeler - SHIELD LINE LLC (078518916)