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.

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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

Package Code 79147-011-01Package Code 79147-011-02

SD NATURALS HAND SANITIZER FRESH CITRUS 
alcohol spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 79147-011
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
HYALURONIC ACID (UNII: S270N0TRQY)  
ALOE (UNII: V5VD430YW9)  
GLYCERIN (UNII: PDC6A3C0OX)  
ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 79147-011-0212 in 1 BOX03/24/2021
1NDC: 79147-011-0159 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00303/24/202112/01/2022
Labeler - SPA DENT INC. (203478896)
Establishment
NameAddressID/FEIBusiness Operations
SPA DENT INC.203478896manufacture(79147-011) , pack(79147-011) , label(79147-011)

Revised: 1/2024
 

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