GERMSTARNORO- ethyl alcohol solution
Soaptronic, LLC

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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germstarNORO

Active ingredient

Ethyl alcohol 63% (W/W)

Purpose

Antiseptic

Uses

Kills 99.99% of all disease causing germs on contact, and protects and restores moisture.

Warnings
For external use only. Keep out of eyes. In case of eye contact immediately flush eyes with water. If irritation persists, get medical attention. If swallowed, contact physician. Flammable, keep away from heat or flames. Germstar Wipes are safe for most surfaces, however can be harmful to some. Test wipe on a non-conspicuous area if unsure.

Keep out of reach of children.

Directions

Apply Germstar all over the surface of your hands and rub into skin until dry. Supervise children in the use of this product.

Other information

Germstar is non allergenic. Store at 20° to 25°C (68° to 77°F). May be harmful to some surfaces/materials.

Inactive ingredients

Water, Isopropanol, Emollient Complex, Fragrance

Questions?

Call Germstar at 1-800.327.2606

Germstar Noro

GERMSTARNORO
ethyl alcohol solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:57915-002
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	630 g in 1000 g

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:57915-002-01	946 g in 1 BAG; Type 0: Not a Combination Product	01/01/2000	05/08/2020
2	NDC:57915-002-02	474 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	01/01/2000	05/08/2020
3	NDC:57915-002-03	236 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/01/2000	05/15/2020
4	NDC:57915-002-04	59 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/01/2000	05/15/2020
5	NDC:57915-002-05	8 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/01/2000	05/15/2020

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333E	01/01/2000	05/15/2020

Labeler - Soaptronic, LLC (082741674)

Registrant - Soaptronic, LLC (082741674)

Name	Address	ID/FEI	Business Operations
Establishment
Soaptronic, LLC		082741674	manufacture(57915-002)

Revised: 5/2020

Document Id: a5efc4e4-2c72-7aa3-e053-2995a90ad54b

Set id: 7733bc43-835f-4c00-82dd-0af78a31a0ff

Version: 12

Effective Time: 20200518

Soaptronic, LLC