Label: HAND SANITIZER- RINSE-FREE gel
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Contains inactivated NDC Code(s)
NDC Code(s): 75129-001-01, 75129-001-02, 75129-001-03, 75129-001-04, view more75129-001-05, 75129-001-06, 75129-001-07, 75129-001-08, 75129-001-09, 75129-001-10, 75129-001-11, 75129-001-12, 75129-001-13 - Packager: Shanghai Rayshine ENVI-TECH Developing CO., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not 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 May 17, 2020
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 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
HAND SANITIZER (RINSE-FREE)
hand sanitizer (rinse-free) gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:75129-001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 62 mL in 100 mL Inactive Ingredients Ingredient Name Strength CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) TROLAMINE (UNII: 9O3K93S3TK) GLYCERIN (UNII: PDC6A3C0OX) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:75129-001-01 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/18/2020 2 NDC:75129-001-02 50 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/18/2020 3 NDC:75129-001-03 54 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/18/2020 4 NDC:75129-001-04 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/18/2020 5 NDC:75129-001-05 80 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/18/2020 6 NDC:75129-001-06 90 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/18/2020 7 NDC:75129-001-07 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/18/2020 8 NDC:75129-001-08 250 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/18/2020 9 NDC:75129-001-09 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/18/2020 10 NDC:75129-001-10 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/18/2020 11 NDC:75129-001-11 2000 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/18/2020 12 NDC:75129-001-12 3785 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/18/2020 13 NDC:75129-001-13 5000 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/18/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/18/2020 Labeler - Shanghai Rayshine ENVI-TECH Developing CO., Ltd. (420836386) Registrant - Shanghai Rayshine ENVI-TECH Developing CO., Ltd. (420836386) Establishment Name Address ID/FEI Business Operations Shanghai Rayshine ENVI-TECH Developing CO., Ltd. 420836386 manufacture(75129-001)
