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Sodium Lauryl Sulfate
  • FDA Inactive Ingredient Details

  • DESCRIPTION

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  • FDA Inactive Ingredient Details
  • DESCRIPTION

FDA INACTIVE INGREDIENT DATABASE

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SODIUM LAURYL SULFATE

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TABLET
BUCCAL
151213
368GB5141J
5.18
MG

FDA INACTIVE INGREDIENT DATABASE

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SODIUM LAURYL SULFATE

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TABLET, EXTENDED RELEA...
BUCCAL
151213
368GB5141J
5.18
MG

FDA INACTIVE INGREDIENT DATABASE

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SODIUM LAURYL SULFATE

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TABLET
BUCCAL/SUBLINGUAL
151213
368GB5141J
1.1
MG

FDA INACTIVE INGREDIENT DATABASE

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SODIUM LAURYL SULFATE

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GEL
DENTAL
151213
368GB5141J
1.47
%

FDA INACTIVE INGREDIENT DATABASE

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SODIUM LAURYL SULFATE

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PASTE
DENTAL
151213
368GB5141J
0
NA

FDA INACTIVE INGREDIENT DATABASE

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SODIUM LAURYL SULFATE

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POWDER
INHALATION
151213
368GB5141J
0
NA

FDA INACTIVE INGREDIENT DATABASE

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SODIUM LAURYL SULFATE

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CAPSULE
ORAL
151213
368GB5141J
25.8
MG

FDA INACTIVE INGREDIENT DATABASE

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SODIUM LAURYL SULFATE

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CAPSULE (IMMED./COMP. ...
ORAL
151213
368GB5141J
3.6
MG

FDA INACTIVE INGREDIENT DATABASE

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SODIUM LAURYL SULFATE

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CAPSULE, DELAYED ACTIO...
ORAL
151213
368GB5141J
5.08
MG

FDA INACTIVE INGREDIENT DATABASE

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SODIUM LAURYL SULFATE

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CAPSULE, DELAYED ACTIO...
ORAL
151213
368GB5141J
2
MG

https://www.pharmacompass.com/pdf-document/pubchem/Sodium-Lauryl-Sulfate-Excipient-pubchem-1495865854.pdf

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