ANTIBACTERIAL DREAMY FLORALS- glycerin soap ANTIBACTERIAL FRUITY ZEST- glycerin soap ANTIBACTERIAL COOLING BREEZE- glycerin soap ANTIBACTERIAL DELIGHTFUL SWEETNESS- glycerin soap ANTIBACTERIAL BOLD CITRUS- glycerin soap

ANTIBACTERIAL BOLD CITRUS by

Drug Labeling and Warnings

ANTIBACTERIAL BOLD CITRUS by is a Otc medication manufactured, distributed, or labeled by Quimicas Handal de Centroamerica SA de CV. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOSAGE & ADMINISTRATION

Pump Caviani hand soap into hands and lather vigorously, from your wrist to your
fingertips. Rinse thoroughly to remove soap. Complete these steps in 20 seconds, repeat if
necessary.

INDICATIONS & USAGE

Pump Caviani hand soap into hands and lather vigorously, from your wrist to your
fingertips. Rinse thoroughly to remove soap. Complete these steps in 20 seconds, repeat if
necessary.

WARNINGS

Avoid contact with eyes. Hold eye open
and rinse slowly and gently with water. Minors
should be supervised while using this product. KEEP
OUT OF REACH OF CHILDREN.
IN CASE OF INGESTION: Rinse mouth with water, seek
amedical assistance.
IN CASE OF INTOXICATION: CONSULT YOUR
DOCTOR AND PROVIDE THIS LABEL.

INACTIVE INGREDIENT

INACTIVE INGREDIENTS: Aqua, Sodium Laureth Sulfate, Sodium
chloride, Sodium Lauroyl Sarcosinate,
Cocamide DEA, Methylchloroisothiazolinone,
Paum, Citric Acid, Tetrasodium EDTA, CI 60725, CI
17200.

KEEP OUT OF REACH OF CHILDREN

Minors
should be supervised while using this product. KEEP
OUT OF REACH OF CHILDREN.

PURPOSE

enhanced protection against germs and delivers
lasting nourishment.

ACTIVE INGREDIENT

GLYCERIN

83033-0010

83033-0020

83033-0030

83033-0040

83033-0050

83033-0060

83033-0070

83033-0080

83033-0090

83033-0100

INGREDIENTS AND APPEARANCE

ANTIBACTERIAL DREAMY FLORALS 
glycerin soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83033-0010
Route of Administration	TRANSDERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	1 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	1 g  in 1 g
SODIUM CHLORIDE (UNII: 451W47IQ8X)	1 g  in 1 g
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)	1 g  in 1 g
SODIUM LAURYL SARCOSINATE (UNII: 5PGH842FAU)	1 g  in 1 g
COCO DIETHANOLAMIDE (UNII: 92005F972D)	1 g  in 1 g
EDETATE SODIUM (UNII: MP1J8420LU)	1 g  in 1 g
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)	1 g  in 1 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83033-0010-1	300 g in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	11/11/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	11/11/2022

ANTIBACTERIAL FRUITY ZEST 
glycerin soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83033-0090
Route of Administration	TRANSDERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	1 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	1 g  in 1 g
WATER (UNII: 059QF0KO0R)	1 g  in 1 g
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)	1 g  in 1 g
SODIUM LAURYL SARCOSINATE (UNII: 5PGH842FAU)	1 g  in 1 g
EDETATE SODIUM (UNII: MP1J8420LU)	1 g  in 1 g
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)	1 g  in 1 g
COCO DIETHANOLAMIDE (UNII: 92005F972D)	1 g  in 1 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83033-0090-1	500 g in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	11/11/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	11/11/2022

ANTIBACTERIAL COOLING BREEZE 
glycerin soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83033-0050
Route of Administration	TRANSDERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	1 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	1 g  in 1 g
SODIUM CHLORIDE (UNII: 451W47IQ8X)	1 g  in 1 g
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)	1 g  in 1 g
SODIUM LAURYL SARCOSINATE (UNII: 5PGH842FAU)	1 g  in 1 g
EDETATE SODIUM (UNII: MP1J8420LU)	1 g  in 1 g
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)	1 g  in 1 g
COCO DIETHANOLAMIDE (UNII: 92005F972D)	1 g  in 1 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83033-0050-1	300 g in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	11/11/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	11/11/2022

ANTIBACTERIAL DREAMY FLORALS 
glycerin soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83033-0060
Route of Administration	TRANSDERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	1 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	1 g  in 1 g
SODIUM CHLORIDE (UNII: 451W47IQ8X)	1 g  in 1 g
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)	1 g  in 1 g
SODIUM LAURYL SARCOSINATE (UNII: 5PGH842FAU)	1 g  in 1 g
EDETATE SODIUM (UNII: MP1J8420LU)	1 g  in 1 g
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)	1 g  in 1 g
COCO DIETHANOLAMIDE (UNII: 92005F972D)	1 g  in 1 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83033-0060-1	500 g in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	11/11/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	11/11/2022

ANTIBACTERIAL COOLING BREEZE 
glycerin soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83033-0100
Route of Administration	TRANSDERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	1 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	1 g  in 1 g
SODIUM CHLORIDE (UNII: 451W47IQ8X)	1 g  in 1 g
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)	1 g  in 1 g
SODIUM LAURYL SARCOSINATE (UNII: 5PGH842FAU)	1 g  in 1 g
EDETATE SODIUM (UNII: MP1J8420LU)	1 g  in 1 g
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)	1 g  in 1 g
COCO DIETHANOLAMIDE (UNII: 92005F972D)	1 g  in 1 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83033-0100-1	500 g in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	11/11/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	11/11/2022

ANTIBACTERIAL FRUITY ZEST 
glycerin soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83033-0040
Route of Administration	TRANSDERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	1 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	1 g  in 1 g
SODIUM CHLORIDE (UNII: 451W47IQ8X)	1 g  in 1 g
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)	1 g  in 1 g
SODIUM LAURYL SARCOSINATE (UNII: 5PGH842FAU)	1 g  in 1 g
EDETATE SODIUM (UNII: MP1J8420LU)	1 g  in 1 g
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)	1 g  in 1 g
COCO DIETHANOLAMIDE (UNII: 92005F972D)	1 g  in 1 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83033-0040-1	300 g in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	11/11/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	11/11/2022

ANTIBACTERIAL DELIGHTFUL SWEETNESS 
glycerin soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83033-0080
Route of Administration	TRANSDERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	1 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	1 g  in 1 g
SODIUM CHLORIDE (UNII: 451W47IQ8X)	1 g  in 1 g
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)	1 g  in 1 g
SODIUM LAURYL SARCOSINATE (UNII: 5PGH842FAU)	1 g  in 1 g
EDETATE SODIUM (UNII: MP1J8420LU)	1 g  in 1 g
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)	1 g  in 1 g
COCO DIETHANOLAMIDE (UNII: 92005F972D)	1 g  in 1 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83033-0080-1	500 g in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	11/11/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	11/11/2022

ANTIBACTERIAL DELIGHTFUL SWEETNESS 
glycerin soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83033-0030
Route of Administration	TRANSDERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	1 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	1 g  in 1 g
SODIUM CHLORIDE (UNII: 451W47IQ8X)	1 g  in 1 g
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)	1 g  in 1 g
SODIUM LAURYL SARCOSINATE (UNII: 5PGH842FAU)	1 g  in 1 g
EDETATE SODIUM (UNII: MP1J8420LU)	1 g  in 1 g
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)	1 g  in 1 g
COCO DIETHANOLAMIDE (UNII: 92005F972D)	1 g  in 1 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83033-0030-1	300 g in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	11/11/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	11/11/2022

ANTIBACTERIAL BOLD CITRUS 
glycerin soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83033-0020
Route of Administration	TRANSDERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	1 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	1 g  in 1 g
SODIUM CHLORIDE (UNII: 451W47IQ8X)	1 g  in 1 g
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)	1 g  in 1 g
SODIUM LAURYL SARCOSINATE (UNII: 5PGH842FAU)	1 g  in 1 g
EDETATE SODIUM (UNII: MP1J8420LU)	1 g  in 1 g
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)	1 g  in 1 g
COCO DIETHANOLAMIDE (UNII: 92005F972D)	1 g  in 1 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83033-0020-1	300 g in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	11/11/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	11/11/2022

ANTIBACTERIAL BOLD CITRUS 
glycerin soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83033-0070
Route of Administration	TRANSDERMAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	1 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	1 g  in 1 g
SODIUM CHLORIDE (UNII: 451W47IQ8X)	1 g  in 1 g
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)	1 g  in 1 g
SODIUM LAURYL SARCOSINATE (UNII: 5PGH842FAU)	1 g  in 1 g
EDETATE SODIUM (UNII: MP1J8420LU)	1 g  in 1 g
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)	1 g  in 1 g
COCO DIETHANOLAMIDE (UNII: 92005F972D)	1 g  in 1 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83033-0070-1	500 g in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	11/11/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	11/11/2022

Labeler - Quimicas Handal de Centroamerica SA de CV (850638768)

Registrant - Quimicas Handal de Centroamerica SA de CV (850638768)

Establishment
Name	Address	ID/FEI	Business Operations
Quimicas Handal de Centroamerica SA de CV		850638768	manufacture(83033-0010, 83033-0020, 83033-0030, 83033-0040, 83033-0050, 83033-0060, 83033-0070, 83033-0080, 83033-0090, 83033-0100) , label(83033-0010, 83033-0020, 83033-0030, 83033-0040, 83033-0050, 83033-0060, 83033-0070, 83033-0080, 83033-0090, 83033-0100)