DISINFECTANT SPRAY WITH pure SILVER

DISINFECTANT WITH pure SILVER by

Drug Labeling and Warnings

DISINFECTANT WITH pure SILVER by is a Otc medication manufactured, distributed, or labeled by RFH BioTek Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DISINFECTANT WITH PURE SILVER- silver spray 
RFH BioTek Inc.

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.

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DISINFECTANT SPRAY WITH pure SILVER

ACTIVE INGREDIENTS

Silver 0.10%

PURPOSE

Antiseptic, Anti-bacterial, Antimicrobial, Anti-viral

USE

This anti-bacterial spray provides an anti-microbial protection film on surfaces. Reduces bacterial growth through silver ions released from MicroSilver. Immediately reduces unpleasant odors and refreshes.

WARNINGS

For external use only

DO NOT USE

On children less than 2 months of age. Avoid contact with broken skin.

WHEN USING THIS PRODUCT

Keep out of eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

STOP USE AND ASK A DOCTOR

If irritation or rash appears and lasts.

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help and contact a Poison Control Centre right away.

DIRECTIONS

Shake well before use. Spray surface from approx. 8 inches away. Supervise children under 6 years of age.

OTHER INFORMATION

Store in a cool, dry place, keep away from direct sunlight. Store between 15-30C (59-86F). Avoid Freezing and excess heat above 40C (104F).

INACTIVE INGREDIENTS

Water, Glycerin, Parfum, Propylene glycol, Ethylhexylglycerin, Sclerotium gum.

DISINFECTANT SPRAY WITH pure SILVER

• Anti-bacterial protection film for surfaces
• Ideal for use on textiles
• Improves hygiene by inhibiting bacterial growth
• Anti-odor complex

MicroSilver

BG™

99.99%

ANTBACTERIAL

DISINFECTANT WITH PURE SILVER 
silver spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78994-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SILVER (UNII: 3M4G523W1G) (SILVER - UNII:3M4G523W1G)	SILVER	0.05 g  in 50 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
BETASIZOFIRAN (UNII: 2X51AD1X3T)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78994-001-01	50 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/18/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		06/18/2020	09/02/2022

Labeler - RFH BioTek Inc. (204177948)

Registrant - RFH BioTek Inc. (204177948)

Revised: 9/2022

Document Id: e7a282e0-f5e7-e811-e053-2995a90ab03c

34390-5

Set id: a8482bf8-d6cc-cae5-e053-2a95a90a8410

Version: 4

Effective Time: 20220901