Label: SYMMETRY HAND SANITIZER- alcohol liquid
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NDC Code(s):
30805-001-01,
30805-001-03,
30805-001-04,
30805-001-06, view more30805-001-07, 30805-001-09, 30805-001-12
- Packager: Buckeye International, 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 November 16, 2020
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
- STORAGE AND HANDLING
- INACTIVE INGREDIENT
- QUESTIONS
- PURPOSE
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
SYMMETRY HAND SANITIZER
alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:30805-001 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 WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) ALOE (UNII: V5VD430YW9) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:30805-001-03 2000 mL in 1 BAG; Type 0: Not a Combination Product 11/16/2007 2 NDC:30805-001-04 1200 mL in 1 BAG; Type 0: Not a Combination Product 11/16/2007 3 NDC:30805-001-06 59.2 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 11/16/2007 4 NDC:30805-001-12 473 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/06/2020 5 NDC:30805-001-07 550 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/23/2020 6 NDC:30805-001-09 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/23/2020 7 NDC:30805-001-01 0.9 mL in 1 PACKET; Type 0: Not a Combination Product 11/16/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 11/16/2007 Labeler - Buckeye International, Inc. (077132280) Establishment Name Address ID/FEI Business Operations Buckeye International, Inc. 077132280 manufacture(30805-001)