Label: NOT HAVE- hand sanitizer gel
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Contains inactivated NDC Code(s)
NDC Code(s): 75439-001-01, 75439-001-02, 75439-001-03, 75439-001-04, view more75439-001-05, 75439-001-06, 75439-001-07, 75439-001-08 - Packager: Guangzhou Yucaitang Cosmetics Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
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 April 22, 2020
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- WARNINGS
- DO NOT USE
- When using this product
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- Directions
- Other Information
- INACTIVE INGREDIENTS
- Package Label - Principal Display Panel
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INGREDIENTS AND APPEARANCE
NOT HAVE
hand sanitizer gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75439-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 73 mL in 100 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) WATER (UNII: 059QF0KO0R) TROLAMINE (UNII: 9O3K93S3TK) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75439-001-01 5 mL in 1 BAG; Type 0: Not a Combination Product 05/05/2020 2 NDC:75439-001-02 50 mL in 1 AMPULE; Type 0: Not a Combination Product 05/05/2020 3 NDC:75439-001-03 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/05/2020 4 NDC:75439-001-04 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/05/2020 5 NDC:75439-001-05 200 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/05/2020 6 NDC:75439-001-06 300 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/05/2020 7 NDC:75439-001-07 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/05/2020 8 NDC:75439-001-08 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/05/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 05/05/2020 Labeler - Guangzhou Yucaitang Cosmetics Co., Ltd. (526897391) Registrant - Guangzhou Yucaitang Cosmetics Co., Ltd. (526897391) Establishment Name Address ID/FEI Business Operations Guangzhou Yucaitang Cosmetics Co., Ltd. 526897391 manufacture(75439-001)