Al CaFoam is a Topical Liquid in the Human Otc Drug category. It is labeled and distributed by Apple Products, Inc.. The primary component is Alcohol.
Product ID | 67147-585_b8a35dcd-dba7-46d8-91f7-79c09b97eb87 |
NDC | 67147-585 |
Product Type | Human Otc Drug |
Proprietary Name | Al CaFoam |
Generic Name | Alcohol |
Dosage Form | Liquid |
Route of Administration | TOPICAL |
Marketing Start Date | 2010-12-01 |
Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
Application Number | part333E |
Labeler Name | Apple Products, Inc. |
Substance Name | ALCOHOL |
Active Ingredient Strength | 1 mL/mL |
NDC Exclude Flag | E |
Listing Certified Through | 2018-12-31 |
Marketing Start Date | 2010-12-01 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-12-01 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-12-01 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-12-01 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-12-01 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-12-01 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-12-01 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-12-01 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-12-01 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-12-01 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-12-01 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-12-01 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-12-01 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-12-01 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-12-01 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-12-01 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-12-01 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-12-01 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-12-01 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-12-01 |
Inactivation Date | 2020-01-31 |
Marketing Category | OTC monograph not final |
Application Number | part333E |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-12-01 |
Inactivation Date | 2020-01-31 |
Ingredient | Strength |
---|---|
ALCOHOL | .7 mL/mL |
SPL SET ID: | 9468ed19-98e6-480b-a8c1-765ef522e794 |
Manufacturer | |
UNII |
NDC | Brand Name | Generic Name |
---|---|---|
67147-658 | Al CaFoam | Al CaFoam |
67147-855 | Al CaFoam | Al CaFoam |
67147-585 | Al CaFoam | Al CaFoam |
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0404-0122 | Antibacterial | alcohol |
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0362-6001 | SeptoSan | Alcohol |
0362-6002 | SeptoSan | Alcohol |
0064-1050 | TRISEPTIN | ALCOHOL |
0363-1305 | Walgreens | Alcohol |
0363-1306 | Walgreens | Alcohol |
0363-1307 | Walgreens | Alcohol |
0363-1308 | Walgreens | Alcohol |
0363-1309 | Walgreens | Alcohol |
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0363-9006 | Walgreens Hand Sanitizer Coastal Breeze Scent | Alcohol |
0363-9007 | Walgreens Hand Sanitizer Crisp Apple Scent | Alcohol |