Label: MOTION SICKNESS- motion sickness patch patch
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NDC Code(s):
83632-001-01,
83632-001-02,
83632-001-03,
83632-001-04, view more83632-001-05, 83632-001-06, 83632-001-07, 83632-001-08, 83632-001-09, 83632-001-10
- Packager: Zhengzhou Zhuoqing Trading Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated August 15, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
- Do not use
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other information
- Inactive ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MOTION SICKNESS
motion sickness patch patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83632-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 2 g in 100 Inactive Ingredients Ingredient Name Strength BORNEOL (UNII: M89NIB437X) GINGER (UNII: C5529G5JPQ) POLYTETRAFLUOROETHYLENE (UNII: E1NC1JVS3O) CHITIN (UNII: 8SH93A7QWW) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83632-001-01 24 in 1 BOX; Type 0: Not a Combination Product 08/16/2023 2 NDC:83632-001-02 36 in 1 BOX; Type 0: Not a Combination Product 08/16/2023 3 NDC:83632-001-03 48 in 1 BOX; Type 0: Not a Combination Product 08/16/2023 4 NDC:83632-001-04 10 in 1 BOX; Type 0: Not a Combination Product 08/16/2023 5 NDC:83632-001-05 20 in 1 BOX; Type 0: Not a Combination Product 08/16/2023 6 NDC:83632-001-06 30 in 1 BOX; Type 0: Not a Combination Product 08/16/2023 7 NDC:83632-001-07 10 in 1 BOX; Type 0: Not a Combination Product 08/16/2023 8 NDC:83632-001-08 20 in 1 BOX; Type 0: Not a Combination Product 08/16/2023 9 NDC:83632-001-09 30 in 1 BOX; Type 0: Not a Combination Product 08/16/2023 10 NDC:83632-001-10 40 in 1 BOX; Type 0: Not a Combination Product 08/16/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 08/16/2023 Labeler - Zhengzhou Zhuoqing Trading Co., Ltd. (713814647) Establishment Name Address ID/FEI Business Operations Zhengzhou Zhuoqing Trading Co., Ltd. 713814647 manufacture(83632-001)