Label: HAND SANITIZER- alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 81191-003-01, 81191-003-02, 81191-003-03, 81191-003-04, view more81191-003-05, 81191-003-06, 81191-003-07, 81191-003-08, 81191-003-09, 81191-003-10, 81191-003-11, 81191-003-12, 81191-003-13, 81191-003-14, 81191-003-15, 81191-003-16, 81191-003-17, 81191-003-18, 81191-003-19, 81191-003-20, 81191-003-21, 81191-003-22, 81191-003-23, 81191-003-24 - Packager: Zhongrong Technology Corporation 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 December 14, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredient(s)
- Purpose
- Use
- Warnings
- Do not use
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WHEN USING
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. - 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
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:81191-003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 75 mL in 100 mL Inactive Ingredients Ingredient Name Strength TROLAMINE (UNII: 9O3K93S3TK) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) PROPYLENE GLYCOL 1,2-DISTEARATE (UNII: T65PN3O37H) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:81191-003-01 30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 11/26/2020 2 NDC:81191-003-02 50 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 11/26/2020 3 NDC:81191-003-03 60 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 11/26/2020 4 NDC:81191-003-04 80 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 11/26/2020 5 NDC:81191-003-05 100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 11/26/2020 6 NDC:81191-003-06 150 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 11/26/2020 7 NDC:81191-003-07 200 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 11/26/2020 8 NDC:81191-003-08 236 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 11/26/2020 9 NDC:81191-003-09 240 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 11/26/2020 10 NDC:81191-003-10 250 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 11/26/2020 11 NDC:81191-003-11 300 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 11/26/2020 12 NDC:81191-003-12 500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 11/26/2020 13 NDC:81191-003-13 600 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 11/26/2020 14 NDC:81191-003-14 800 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 11/26/2020 15 NDC:81191-003-15 900 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 11/26/2020 16 NDC:81191-003-16 1000 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 11/26/2020 17 NDC:81191-003-17 2000 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 11/26/2020 18 NDC:81191-003-18 3780 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/26/2020 19 NDC:81191-003-19 5000 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/26/2020 20 NDC:81191-003-20 10000 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/26/2020 21 NDC:81191-003-21 100000 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/26/2020 22 NDC:81191-003-22 200000 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/26/2020 23 NDC:81191-003-23 1000000 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/26/2020 24 NDC:81191-003-24 2500 mL in 1 BOTTLE; Type 0: Not a Combination Product 11/26/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 11/26/2020 Labeler - Zhongrong Technology Corporation Ltd. (529575698) Registrant - Zhongrong Technology Corporation Ltd. (529575698) Establishment Name Address ID/FEI Business Operations Zhongrong Technology Corporation Ltd. 529575698 manufacture(81191-003) , label(81191-003)
