Alert Re: “WAVE”-Branded Hand Sanitizer
To our Valued Customers and Distributors:
You may be aware of a recent alert issued by the Food and Drug
Administration (the "FDA") concerning "WAVE"-branded hand
sanitizer sold by C&A Marketing, Inc. ("C&A").
At no time has C&A purchased or manufactured any product from
Tropicosmeticos SA de CV or any other supplier based in Mexico,
whether under the “WAVE” brand or any other brand. The FDA’s
alert regarding WAVE hand sanitizer was issued in error and we are
in discussions with the FDA towards retracting the WAVE advisory.
Please be assured that WAVE-branded hand sanitizer and all
ingredients therein are supplied from domestic United States
sources only and is manufactured in the United States. Our safety
data sheet and registration with the FDA is available to you upon
request.
If you have any questions regarding the above, please do not hesitate
to contact us at (848) 244-2075 or wave@caglobal.com
FDA Active Approval Screenshots:
1 Gallon FDA Approved (NDC number: 78754-001-28)
16oz Bottle FDA Approved (NDC number: 78754-001-16)
8oz Bottle FDA Approved (NDC number: 78754-001-08)
Safety Sheet:
Wave MSDS Safety Sheet
Letter From CEO
Letter From CEO of CA Global 8-13-2020
Our Legal Statement:
WAVE Alert Response
We sincerely apologize for any confusion that has arisen due to the recent alert issued by the Food and Drug Administration (FDA) concerning WAVE-branded hand sanitizer. Please be assured that the WAVE product you purchased is not subject to a recall or FDA action and is perfectly safe for use. At no time have we purchased or manufactured any product from Tropicosmeticos SA de CV or any other supplier based in Mexico, whether under our own brand (WAVE) or any other brand. The FDA’s alert regarding our WAVE hand sanitizer was issued in error and we are in discussions with them with regard to retracting said advisory. Please be assured that Wave-branded hand sanitizer and all ingredients therein are supplied from domestic United States sources only and is manufactured and bottled in the United States, all pursuant to FDA registration.
In order to verify that our product appears on the approved FDA's approval list. please click on the below link and follow the instructions.
https://www.accessdata.fda.gov/scripts/cder/ndc/index.cfm and follow these directions:
In the “Select Type” field, select ”Proprietary Name.”
In the field below where you made the "Select Type" selection, type in the words Wave Hand Sanitizer.
You will see a few of our listings. There are multiple listings because each one corresponds to a different sized bottle.
C&A Marketing, Inc. is the corporate name under which these products are manufactured and is our parent company. Southern Lithoplate is one of our approved bottling facilities. Please note that the first few results under the companies "Fresh Wave" and "NOWAVE" are not affiliated with us.