SD NATURALS HAND SANITIZER FRESH CITRUS by SPA DENT INC.

SD NATURALS HAND SANITIZER FRESH CITRUS by

Drug Labeling and Warnings

SD NATURALS HAND SANITIZER FRESH CITRUS by is a Otc medication manufactured, distributed, or labeled by SPA DENT INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SD NATURALS HAND SANITIZER FRESH CITRUS- alcohol spray 
SPA DENT INC.

----------

Active Ingredient(s)

Alcohol 80% v/v. Purpose: Antiseptic

Purpose

Antiseptic, Hand Sanitizer

Use

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

For external use only. Flammable. Keep away from heat or flame

Do not use

• in children less than 2 months of age
• on open skin wounds

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 occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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

Directions

• Place enough product on hands to cover all surfaces. Rub hands together until dry.
• Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

• Store between 15-30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

glycerin, hydrogen peroxide, purified water USP

Package Label - Principal Display Panel

SD NATURALS HAND SANITIZER FRESH CITRUS 
alcohol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79147-011
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
HYALURONIC ACID (UNII: S270N0TRQY)
ALOE (UNII: V5VD430YW9)
GLYCERIN (UNII: PDC6A3C0OX)
ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79147-011-02	12 in 1 BOX	03/24/2021
1	NDC: 79147-011-01	59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	03/24/2021	12/01/2022

Labeler - SPA DENT INC. (203478896)

Establishment
Name	Address	ID/FEI	Business Operations
SPA DENT INC.		203478896	manufacture(79147-011) , pack(79147-011) , label(79147-011)

Revised: 1/2024

Document Id: 0fb4d584-62f4-b271-e063-6294a90ae19d

34390-5

Set id: be4e94bb-7a47-08b3-e053-2995a90aecf0

Version: 4

Effective Time: 20240124