Label: NOT HAVE- antibacterial antiseptic spray spray
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Contains inactivated NDC Code(s)
NDC Code(s): 74761-002-01, 74761-002-02, 74761-002-03, 74761-002-04, view more74761-002-05, 74761-002-06, 74761-002-07, 74761-002-08, 74761-002-09, 74761-002-10, 74761-002-11, 74761-002-12, 74761-002-13, 74761-002-14 - Packager: Guangzhou Oumiao Cosmetics 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 May 3, 2020
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
- Warnings
- DO NOT USE
- When using this product
- STOP USE
- Keep out of reach of children
- Directions
- Other information
- Inactive ingredients
- Package Label - Principal Display Panel
-
INGREDIENTS AND APPEARANCE
NOT HAVE
antibacterial antiseptic spray sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:74761-002 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 WATER (UNII: 059QF0KO0R) POLIHEXANIDE HYDROCHLORIDE (UNII: 4XI6112496) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:74761-002-01 50 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/04/2020 2 NDC:74761-002-02 60 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/04/2020 3 NDC:74761-002-03 80 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/04/2020 4 NDC:74761-002-04 100 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/04/2020 5 NDC:74761-002-05 200 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/04/2020 6 NDC:74761-002-06 250 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/04/2020 7 NDC:74761-002-07 300 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/04/2020 8 NDC:74761-002-08 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/04/2020 9 NDC:74761-002-09 1000 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/04/2020 10 NDC:74761-002-10 2000 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/04/2020 11 NDC:74761-002-11 5000 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/04/2020 12 NDC:74761-002-12 400000 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/04/2020 13 NDC:74761-002-13 800000 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/04/2020 14 NDC:74761-002-14 1000000 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/04/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 05/04/2020 Labeler - Guangzhou Oumiao Cosmetics Co. Ltd. (529806412) Registrant - Guangzhou Oumiao Cosmetics Co. Ltd. (529806412) Establishment Name Address ID/FEI Business Operations Guangzhou Oumiao Cosmetics Co. Ltd. 529806412 manufacture(74761-002)
