Label: BENZOIN COMPOUND TINCTURE- benzoin resin liquid
- NDC Code(s): 0395-0243-16, 0395-0243-92
- Packager: Humco Holding Group, Inc.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 15, 2023
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active Ingredient
- Purpose
- Use
- Warnings
- When using this product
- Stop use and consult a dentist or doctor if
- Keep out of reach of children.
- Directions
- Other information
- Inactive Ingredients
- Principal Display Panel - 16oz
- Principal Display Panel - 2 oz
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INGREDIENTS AND APPEARANCE
BENZOIN COMPOUND TINCTURE
benzoin resin liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0395-0243 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZOIN RESIN (UNII: GK21SBA74R) (BENZOIN RESIN - UNII:GK21SBA74R) BENZOIN RESIN 1000 mg in 1 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) ALOE (UNII: V5VD430YW9) TOLU BALSAM (UNII: TD2LE91MBE) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0395-0243-16 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/10/2017 2 NDC:0395-0243-92 59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/10/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M022 01/01/2008 Labeler - Humco Holding Group, Inc. (825672884) Registrant - Pharma Nobis, LLC (118564114) Establishment Name Address ID/FEI Business Operations Pharma Nobis, LLC 118564114 manufacture(0395-0243) , analysis(0395-0243) , pack(0395-0243) , label(0395-0243)