Spatherapy Antibacterial Hand Spray

Spatherapy Antibacterial Hand by

Drug Labeling and Warnings

Spatherapy Antibacterial Hand by is a Otc medication manufactured, distributed, or labeled by Shalom International Corp. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPATHERAPY ANTIBACTERIAL HAND- alcohol spray 
Shalom International Corp

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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Spatherapy Antibacterial Hand Spray

Drug Facts

Active Ingredients

Alcohol Denat. 62%

Purpose

Antibacterial

Uses

  • Hand sanitizer to help reduce bacteria on the skin that could cause disease.
  • Recommended for repeated use.

Warnings

  • Flamable. Keep away from fire or flame.
  • For external use only

When using this product

do not use in or near the eyes. Incase of contact, rinse eyes thoroughly with water.

Stop use & ask a doctor

If irritation or rash appears and lasts.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Apply enough product to thoroughly cover hands.
  • Rub hands together briskly until dry.

Other Information

  • Do not store above 110°F (43°C).
  • May discolor certain fabrics or surfaces.

Inactive Ingredients

Water (Aqua), PEG-40 Hydrogenated Castor Oil, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, DMDM Hydantoin, Fragrance(Parfum), Sodium Hydroxide, Aloe Barbadensis Leaf Extract, Tocopheryl Acetate.

Questions?

  • Call 212-391-6970

Package Labeling

Bottle6

SPATHERAPY ANTIBACTERIAL HAND 
alcohol spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 73025-064
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.62 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
DMDM HYDANTOIN (UNII: BYR0546TOW)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 73025-064-00118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product07/01/202012/31/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E07/01/202012/31/2021
Labeler - Shalom International Corp (001384825)

Revised: 3/2022