Label: REDNESS RELIEVER- tetrahydrozoline hcl liquid
- NDC Code(s): 41520-531-05
- Packager: American Sales Company
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated February 17, 2023
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- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Use
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Warnings
When using this product
- pupils may become enlarged temporarily
- to avoid contamination, do not touch tip of container to any surface. Replace cap after using.
- if solution changes color or becomes cloudy, do not use
- overuse may produce increased redness of the eye
- remove contact lenses before using
- pupils may become enlarged temporarily
- Directions
- Other information
- Inactive ingredients
- package label
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INGREDIENTS AND APPEARANCE
REDNESS RELIEVER
tetrahydrozoline hcl liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41520-531 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TETRAHYDROZOLINE HYDROCHLORIDE (UNII: 0YZT43HS7D) (TETRAHYDROZOLINE - UNII:S9U025Y077) TETRAHYDROZOLINE HYDROCHLORIDE 0.5 mg in 1 mL Inactive Ingredients Ingredient Name Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) BORIC ACID (UNII: R57ZHV85D4) HYDROCHLORIC ACID (UNII: QTT17582CB) EDETATE DISODIUM (UNII: 7FLD91C86K) WATER (UNII: 059QF0KO0R) SODIUM BORATE (UNII: 91MBZ8H3QO) SODIUM CHLORIDE (UNII: 451W47IQ8X) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41520-531-05 1 in 1 BOX 09/06/2011 1 15 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part349 09/06/2011 Labeler - American Sales Company (809183973)