PREVICARE  HYSSOP SANITIZER- alcohol gel 
PREVICARE  HOLY WATER PLUS HYSSOP SANITIZER- alcohol gel 
Previcare Pharmaceutical, Inc.

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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Previcare Hyssop Sanitizer Gel

Drug Facts

Active Ingredient

Ethyl Alcohol 70% V/V

Purpose

Antiseptic

Uses

Hand sanitizer to help reduce bacteria that potentially 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 ingest. Do not use if you are allergic to any ingredient.

Keep out of reach of children. If swallowed, get medical help. Do not use on open wounds. When using ths product avoid contact with eyes. In case of contact with eyes, rinse thoroughly with water. Stop use and ask a doctor if irritation develops.

Directions

Apply to one palm, rub hands together until dry. Use as part of your daily cleaning routine. Do not rinse with water. Do not dilute the product. Supervise children when using this product.

Other Information

Store at 50-86°F (15-30°C).

Inactive Ingredients

Aqua (purified water), Hyssop and Rosemary Mint Oil, Glycerin, Aloe Barbadensis (Aloe) Leaf Juice, PEG-75 Lanolin, PEG-7 Glyceryl Cocoate (emollient), Myristyl Alcohol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Triethanolamine.

Questions?

Call 1 (716) 427-7979

Distributed by: Previcare Pharmaceutical, Inc.
50 Fountain Plaza • Suite 1400 • Buffalo • NY • 14202 • USA

PRINCIPAL DISPLAY PANEL - 60 ML Bottle Label - NDC 73401-849

PREVICARE
SANITIZER GEL | 70% ALCOHOL

HYSSOP

2 FL OZ (60 ML)

NDC 73401-849-09

Principal Display Panel - 60 ML Bottle Label - NDC 73401-849

PRINCIPAL DISPLAY PANEL - 60 ML Bottle Label - NDC 73401-850

PREVICARE
SANITIZER GEL | 70% ALCOHOL

HOLY WATER
+ HYSSOP

2 FL OZ (60 ML)

NDC 73401-850-09

Principal Display Panel - 60 ML Bottle Label - NDC 73401-850
PREVICARE   HYSSOP SANITIZER
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73401-849
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
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
PEG-75 LANOLIN (UNII: 09179OX7TB)  
MYRISTYL ALCOHOL (UNII: V42034O9PU)  
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
TROLAMINE (UNII: 9O3K93S3TK)  
PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)  
HYSSOP OIL (UNII: 173D71924B)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73401-849-0960 mL in 1 BOTTLE; Type 0: Not a Combination Product02/15/2021
2NDC:73401-849-1060 mL in 1 BOTTLE; Type 0: Not a Combination Product02/17/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart333A02/15/2021
PREVICARE   HOLY WATER PLUS HYSSOP SANITIZER
alcohol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73401-850
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
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
PEG-75 LANOLIN (UNII: 09179OX7TB)  
MYRISTYL ALCOHOL (UNII: V42034O9PU)  
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
TROLAMINE (UNII: 9O3K93S3TK)  
PEG-7 GLYCERYL COCOATE (UNII: VNX7251543)  
HYSSOP OIL (UNII: 173D71924B)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:73401-850-0960 mL in 1 BOTTLE; Type 0: Not a Combination Product02/15/2021
2NDC:73401-850-1060 mL in 1 BOTTLE; Type 0: Not a Combination Product02/17/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart333A02/15/2021
Labeler - Previcare Pharmaceutical, Inc. (117180835)

Revised: 2/2021
Document Id: a16aaf24-d40c-4b9b-9bee-773c57ba749d
Set id: 41d97ec1-4c15-4187-8123-fa3e78156de7
Version: 1
Effective Time: 20210210
 
Previcare Pharmaceutical, Inc.