Puro Azul Awapuhi AntiBac by National Paper Company, Inc.

Puro Azul Awapuhi AntiBac by

Drug Labeling and Warnings

Puro Azul Awapuhi AntiBac by is a Otc medication manufactured, distributed, or labeled by National Paper Company, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PURO AZUL AWAPUHI ANTIBAC- pcmx soap 
National Paper Company, Inc.

----------

Active Ingredient

Chloroxylenol 0.1%

Purpose

Antiseptic

Uses

Handwash to help decrease bacteria on the skin.

Warnings

For external use only.
Do not use in the eyes. In case of contact, immediately flush eyes with water.

Stop use and 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 a small amount of product to wet hands, work into lather for 30 seconds, and rinse thoroughly.
Children under 6 years of age should be supervised when using this product.

Inactive Ingredients

Water (Aqua) (7732-18-5), Sodium Lauryl Sulfate (68585-47-7), Cocamidopropyl Hydroxysultaine (68139-30-0), Sodium Chloride (7647-14-5), Propanediol (26264-14-2), Propylene Glycol (57-55-6), Sodium C14-16 Olefin Sulfonate (68439-57-6), Glycol Distearate (627-83-8), Fragrance (Proprietary), Sodium Citrate (6132-04-3), Dibromocyanoacetamide (10222-01-2), Methylisothiazolinone (2682-20-4), Methylchloroisothiazolinone (26172-55-4), 2-Bromo-2-Nitropropane-1,3-Diol (52-51-7).

PURO AZUL AWAPUHI ANTIBAC 
pcmx soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82076-301
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q)	CHLOROXYLENOL	1 g  in 1 L

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)
DIBROMOCYANOACETAMIDE (UNII: 7N51QGL6MJ)
ALLYL HEXANOATE (UNII: 3VH84A363D)
GLYCOL DISTEARATE (UNII: 13W7MDN21W)
BRONOPOL (UNII: 6PU1E16C9W)
WATER (UNII: 059QF0KO0R)
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
HEXAMETHYLINDANOPYRAN (UNII: 14170060AT)
.GAMMA.-NONALACTONE (UNII: I1XGH66S8P)
ETHYL CAPROATE (UNII: FLO6YR1SHT)
PROPANEDIOL (UNII: 5965N8W85T)
VANILLIN (UNII: CHI530446X)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ALLYL AMYL GLYCOLATE (UNII: EMX89K493E)
COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82076-301-41	3.78 L in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	08/13/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	08/13/2021	01/30/2026

Labeler - National Paper Company, Inc. (035135144)

Revised: 7/2025

Document Id: 3b004b22-ad24-7803-e063-6294a90afe86

34390-5

Set id: c975cadc-e985-664c-e053-2995a90a539f

Version: 7

Effective Time: 20250728