SOLGREAT ANTIBACTERIAL HANDWASH- benzalkonium chloride liquid
PANATURAL USA, INC.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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SolGreat Antibacterial handwash

Active lngredient

Benzalkonium Chloride

Purpose

Antibacterial

Uses

for handwashing to decrease bacteria on the skin.

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 develop.

Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• place enough product into your palms, wet as needed.
• lather vigorously for at least 20 seconds.
• wash skin, rinse and dry thoroughly.

Inactive ingredients

Cetrimonium Chloride, Cocamide Methyl MEA, Lauramine Oxide, Methylchoroisothiazolinone, Methylisothiazolinone, Parfum (Fragrance), Propanediol, Sodium Chloride, Tocopheryl Acetate, FD&C Yellow No. 5, FD&C Red No. 4, Water.

Product Label
237mL SolGreat Antibacterial Hand Soap

237mL

Product Label - 500mL SolGreat Antibacterial Hand Soap

500mL

SOLGREAT ANTIBACTERIAL HANDWASH
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:73913-003
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
Cetrimonium chloride (UNII: UC9PE95IBP)
COCOYL METHYL MONOETHANOLAMINE (UNII: 79G1T427CF)
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
PROPANEDIOL (UNII: 5965N8W85T)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:73913-003-01	237 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/27/2020
2	NDC:73913-003-02	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/27/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	03/23/2020

Labeler - PANATURAL USA, INC. (029572239)

Name	Address	ID/FEI	Business Operations
Establishment
Hefei Yatai Daily-Use Chemical Industry Co., Ltd		654641724	manufacture(73913-003)