Sodium Lauryl Sulfate & SODIUM LAURYL SULFATE Excipient Use in Spray Dosage Forms

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Sodium Lauryl Sulfate

FDA Inactive Ingredient Details, DESCRIPTION

FDA Inactive Ingredient Details
DESCRIPTION

Suppliers

5 Listed Products, 5 BASF

5 Listed Products
5 BASF

REGULATORY FILINGS

3 Suppliers, 3 USDMF

3 Suppliers
3 USDMF

SOLUTIONS BY APPLICATIONS

2 Taste Masking, 2 Granulation, 2 Coating Systems & Additives, 1 Direct Compression, 1 Topical, 1 Controlled & Modified Release, 1 Lubricants & Glidants

2 Taste Masking
2 Granulation
2 Coating Systems & Additives
1 Direct Compression
1 Topical
1 Controlled & Modified Release
1 Lubricants & Glidants

FINISHED FORMULATIONS

1073 ORAL, 466 TABLET, 334 CAPSULE, 80 CAPSULE, EXTENDED RELEASE, 66 TABLET, EXTENDED RELEASE, 43 CAPSULE, DELAYED REL PELLETS, 20 TABLET, DELAYED RELEASE, 19 CAPSULE, DELAYED RELEASE, 17 TOPICAL, 16 FOR SUSPENSION, 10 TABLET, ORALLY DISINTEGRATING, 9 CREAM, 9 TABLET, CHEWABLE, 5 SPRAY, 5 TABLET, FOR SUSPENSION, 4 ORAL-28, 4 SUSPENSION, 3 GRANULE, 2 LOTION, 2 OINTMENT, 2 ORAL-21, 2 SOLUTION, 2 VAGINAL, 1 BUCCAL, 1 DENTAL, 1 FOR SOLUTION, 1 FOR SUSPENSION, DELAYED RELEASE, 1 INJECTABLE, 1 INJECTION, 1 LOTION/SHAMPOO, 1 PASTE, 1 SUSPENSION, EXTENDED RELEASE, 1 VIAL