Label: ALCOHOL PREP PAD- isopropyl alcohol swab
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Contains inactivated NDC Code(s)
NDC Code(s): 50232-001-01, 50232-001-02, 50232-001-03 - Packager: BEIJING RUICHENG MEDICAL SUPPLIES CO., LTD.
- 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.
Drug Label Information
Updated March 19, 2022
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- Active Ingredient
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- Inactive ingredients
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INGREDIENTS AND APPEARANCE
ALCOHOL PREP PAD
isopropyl alcohol swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50232-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 0.7 mL in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50232-001-01 5000 in 1 CONTAINER 01/01/2018 1 0.35 mL in 1 POUCH; Type 0: Not a Combination Product 2 NDC:50232-001-02 10000 in 1 CONTAINER 01/01/2018 2 0.35 mL in 1 POUCH; Type 0: Not a Combination Product 3 NDC:50232-001-03 3000 in 1 CONTAINER 01/01/2018 3 0.35 mL in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part344 05/14/2012 Labeler - BEIJING RUICHENG MEDICAL SUPPLIES CO., LTD. (421285328) Establishment Name Address ID/FEI Business Operations BEIJING RUICHENG MEDICAL SUPPLIES CO., LTD. 421285328 manufacture(50232-001)