Label: OLIKA ULTRA HYDRATING HAND SANITIZER, BOLD- alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 73517-921-02, 73517-921-03 - Packager: Amyris, Inc
- 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 7, 2022
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DO NOT USE
- WHEN USING
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- STORAGE AND HANDLING
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
OLIKA ULTRA HYDRATING HAND SANITIZER, BOLD
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73517-921 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 65 mL in 100 mL Inactive Ingredients Ingredient Name Strength FRAGRANCE 13576 (UNII: 5EM498GW35) GLYCERIN (UNII: PDC6A3C0OX) ALOE VERA LEAF (UNII: ZY81Z83H0X) DENATONIUM BENZOATE (UNII: 4YK5Z54AT2) HYALURONATE SODIUM (UNII: YSE9PPT4TH) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73517-921-02 20 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 05/09/2022 2 NDC:73517-921-03 90 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 05/09/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 05/09/2022 Labeler - Amyris, Inc (185930182) Establishment Name Address ID/FEI Business Operations Taizhou Jingshang Cosmetics Technology Co., Ltd. 550819554 manufacture(73517-921)