Label: LOCKE TEDDY- alcohol antiseptic gel
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NDC Code(s):
73928-001-01,
73928-001-02,
73928-001-03,
73928-001-04, view more73928-001-05, 73928-001-06, 73928-001-07, 73928-001-08, 73928-001-09, 73928-001-10, 73928-001-11, 73928-001-12, 73928-001-13, 73928-001-14
- Packager: KINGKEY MBC LIFE TECHNOLOGY GROUP CO.,LTD
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 29, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active lngredient
- Purpose
- Uses
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Warnings
For external use only. Flammable. Keep away from heat or flame
Do not use
• in children less than 2 months of age
• on open skin wounds
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 ifirritation 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. - Directions
- Other information
- Inactives
- KEEP OUT OF REACH OF CHILDREN
- Product Label
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INGREDIENTS AND APPEARANCE
LOCKE TEDDY
alcohol antiseptic gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73928-001 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 AMINOMETHYLPROPANOL (UNII: LU49E6626Q) WATER (UNII: 059QF0KO0R) CARBOMER 980 (UNII: 4Q93RCW27E) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73928-001-01 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/26/2020 2 NDC:73928-001-02 50 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/26/2020 3 NDC:73928-001-03 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/26/2020 4 NDC:73928-001-04 250 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/26/2020 5 NDC:73928-001-05 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/26/2020 6 NDC:73928-001-06 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/26/2020 7 NDC:73928-001-07 2000 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/26/2020 8 NDC:73928-001-08 200 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/26/2020 9 NDC:73928-001-09 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/26/2020 10 NDC:73928-001-10 150 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/26/2020 11 NDC:73928-001-11 236 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/26/2020 12 NDC:73928-001-12 296 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/26/2020 13 NDC:73928-001-13 300 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/26/2020 14 NDC:73928-001-14 5000 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/26/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M003 03/26/2020 Labeler - KINGKEY MBC LIFE TECHNOLOGY GROUP CO.,LTD (545349263) Establishment Name Address ID/FEI Business Operations KINGKEY MBC LIFE TECHNOLOGY GROUP CO.,LTD 545349263 manufacture(73928-001)