Label: HAND SANITIZER- alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 71011-003-01, 71011-003-02, 71011-003-03, 71011-003-04, view more71011-003-05, 71011-003-06, 71011-003-07, 71011-003-08, 71011-003-09, 71011-003-10, 71011-003-11, 71011-003-12, 71011-003-13, 71011-003-14, 71011-003-15, 71011-003-16, 71011-003-17, 71011-003-18, 71011-003-19, 71011-003-20, 71011-003-21, 71011-003-22, 71011-003-23, 71011-003-24, 71011-003-25, 71011-003-26, 71011-003-27 - Packager: NingBo Huize Commodity 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 January 6, 2018
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient
- Purpose
- Use
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Warning
for external use only
Do not use on broken skin & around eyes
When using this product
■Keep away from fire or flame
■Using other topical acne drugs at the same time or right after use of this product may increase dryness or irritation of the skin . Only one drug should be used unless directed by a doctor. - Directions
- INACTIVE INGREDIENT
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
HAND SANITIZER
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71011-003 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) DMDM HYDANTOIN (UNII: BYR0546TOW) ALOE VERA LEAF (UNII: ZY81Z83H0X) PROPYLENE GLYCOL DIACETATE (UNII: 5Z492UNF9O) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71011-003-01 5 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/20/2016 2 NDC:71011-003-02 8 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/20/2016 3 NDC:71011-003-03 10 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/20/2016 4 NDC:71011-003-04 15 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/20/2016 5 NDC:71011-003-05 20 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/19/2016 6 NDC:71011-003-06 30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/19/2016 7 NDC:71011-003-07 50 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/20/2016 8 NDC:71011-003-08 60 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/20/2016 9 NDC:71011-003-09 80 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/20/2016 10 NDC:71011-003-10 100 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/20/2016 11 NDC:71011-003-11 150 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/20/2016 12 NDC:71011-003-12 200 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/20/2016 13 NDC:71011-003-13 250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/20/2016 14 NDC:71011-003-14 300 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/20/2016 15 NDC:71011-003-15 400 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/20/2016 16 NDC:71011-003-16 500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/20/2016 17 NDC:71011-003-17 600 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/20/2016 18 NDC:71011-003-18 700 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/20/2016 19 NDC:71011-003-19 800 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/20/2016 20 NDC:71011-003-20 900 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/20/2016 21 NDC:71011-003-21 1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/20/2016 22 NDC:71011-003-22 2000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/20/2016 23 NDC:71011-003-23 5 mL in 1 POUCH; Type 0: Not a Combination Product 10/20/2016 24 NDC:71011-003-24 8 mL in 1 POUCH; Type 0: Not a Combination Product 10/20/2016 25 NDC:71011-003-25 25 mL in 1 POUCH; Type 0: Not a Combination Product 10/20/2016 26 NDC:71011-003-26 15 mL in 1 POUCH; Type 0: Not a Combination Product 10/20/2016 27 NDC:71011-003-27 20 mL in 1 POUCH; Type 0: Not a Combination Product 10/20/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 06/09/2016 Labeler - NingBo Huize Commodity Co.,Ltd. (544434795) Establishment Name Address ID/FEI Business Operations NingBo Huize Commodity Co.,Ltd. 544434795 manufacture(71011-003)
