USFDA APPLICATION NUMBER - 204308 / DOSAGE - FOR SOLUTION;ORAL - 1MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Inactive Ingredients
Ingredient Name | Silvergate Pharmaceuticals, Inc. |
---|---|
CITRIC ACID MONOHYDRATE(2968PHW8QP) | |
GLYCERIN(PDC6A3C0OX) | |
MANNITOL(3OWL53L36A) | |
METHYLPARABEN(A2I8C7HI9T) | |
POTASSIUM SORBATE(1VPU26JZZ4) | |
PROPYLPARABEN(Z8IX2SC1OH) | |
SACCHARIN SODIUM(SB8ZUX40TY) | |
SILICON DIOXIDE(ETJ7Z6XBU4) | |
SODIUM CITRATE, UNSPECIFIED FORM(1Q73Q2JULR) | |
SORBITOL(506T60A25R) | |
WATER(059QF0KO0R) | |
XANTHAN GUM(TTV12P4NEE) |
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