Ingredient
Sodium Metabisulfite
SODIUM METABISULFITE appears in 43 FDA IID formulation listing(s).
Also labeled: SODIUM METABISULFITE
In food
Food additive / labeled ingredient
Appears on packaged-food labels and is documented in FDA IID pharmaceutical formulation records.
Identifiers
- UNII: 4VON5FNS3C · verified
- CAS: 7681574 · verified
Also used in
SODIUM METABISULFITE appears in 43 FDA IID formulation listing(s).
43 documented listings · routes: epidural, infiltration, intra-articular, intrabursal, intracardiac, intralesional, intramuscular, intraocular, intraperitoneal, intravenous, iontophoresis, ophthalmic, oral, peridural, perineural, rectal, respiratory (inhalation), subcutaneous, sublingual, submucosal, topical
General medicine
Sodium Metabisulfite
Inactive ingredient
Indicated for the gradual bleaching of hyperpigmented skin conditions such as chloasma, melasma, freckles, senile lentigines, and other unwanted areas of hyperpigmentation.
This does not mean the food ingredient treats general medicine. It means it is documented as an inactive ingredient in this medication formulation.
View documented labelOncology
SHISEIDO ULTIMATE SUN PROTECTOR
Inactive ingredient
Uses helps prevent sunburn if used as directed with other sun protection measures (see Directions ), decreases the risk of skin cancer and early skin aging caused by the sun
This does not mean the food ingredient treats oncology. It means it is documented as an inactive ingredient in this medication formulation.
View documented labelPain
Sodium Metabisulfite
Inactive ingredient
Uses: Temporarily relieves local discomfort or pain and swelling or burning associated with anorectal disorders.
This does not mean the food ingredient treats pain. It means it is documented as an inactive ingredient in this medication formulation.
View documented label
Documented uses
SODIUM METABISULFITE appears in 43 FDA IID formulation listing(s).
This does not mean the food ingredient treats a condition. It means the same or verified equivalent substance is documented in a medication formulation — as an inactive ingredient unless evidence verifies it is active.
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