Label: KUTKIT- aluminum sulfate swab
- NDC Code(s): 10705-301-50
- Packager: Majestic Drug Co., Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Updated January 24, 2022
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- SPL UNCLASSIFIED SECTION
- Active Ingredient
For external use only.
When using this product
- Avoid contact with eyes. If contact occurs rinse thoroughly with water.
- Stings when applied. For minor cuts and scrapes only.
- Inactive Ingredient
- PRINCIPAL DISPLAY PANEL - 24 Swab Box
INGREDIENTS AND APPEARANCE
aluminum sulfate swab
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10705-301 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Aluminum Sulfate (UNII: 34S289N54E) (ALUMINUM SULFATE ANHYDROUS - UNII:I7T908772F) Aluminum Sulfate 0.047 g Inactive Ingredients Ingredient Name Strength Water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10705-301-50 24 in 1 BOX; Type 0: Not a Combination Product 11/07/2020 12/31/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 11/07/2020 12/31/2023 Labeler - Majestic Drug Co., Inc. (001496777)