Label: DIABECLINE- tetracycline hydrochloride ointment
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Contains inactivated NDC Code(s)
NDC Code(s): 43074-112-11 - Packager: Phillips Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph 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 July 12, 2013
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Diabecline Brand Topical Ointment First Aid Antibiotic Tetracycline Hydrochloride 0.1 OZ (3 G)
- Active Ingredient (in each gram)
- Purpose
- use
- Warnings
- Do Not Use
- Ask a doctor before use if you have
- Stop use and ask a doctor
- Keep Out of reach of children
- Directions
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Other Information
Keep product refrigerated to preserve its effectiveness and color.
Stop use if product is misused: If the bottle is left open and/or if not refrigerated, the liquid will tend to turn black over time.
Discard the product if the liquid turns black due to misuse.
This product is an OTC antibiotic for human use.
Contains no alcohol, no animal ingredients.
Blended for typical skin color.
May stain cloth.
No claims regarding stem cell healing are implied for this product.
- INACTIVE INGREDIENTS
- Diabecline Brand Topical Ointment First Aid Antibiotic Tetracycline Hydrochloride 0.1 OZ (3 G)
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INGREDIENTS AND APPEARANCE
DIABECLINE
tetracycline hydrochloride ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:43074-112 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TETRACYCLINE HYDROCHLORIDE (UNII: P6R62377KV) (TETRACYCLINE - UNII:F8VB5M810T) TETRACYCLINE HYDROCHLORIDE 30 mg in 1 g Inactive Ingredients Ingredient Name Strength ASCORBIC ACID (UNII: PQ6CK8PD0R) CHLORHEXIDINE GLUCONATE (UNII: MOR84MUD8E) CHOLECALCIFEROL (UNII: 1C6V77QF41) DIMETHYL SULFOXIDE (UNII: YOW8V9698H) DIPROPYLENE GLYCOL (UNII: E107L85C40) GLUCONOLACTONE (UNII: WQ29KQ9POT) GLYCERIN (UNII: PDC6A3C0OX) HYDROXYMETHYL CELLULOSE (UNII: 273FM27VK1) MAGNESIUM STEARATE (UNII: 70097M6I30) METHYLPARABEN (UNII: A2I8C7HI9T) SODIUM HYDROXIDE (UNII: 55X04QC32I) SORBIC ACID (UNII: X045WJ989B) STEARIC ACID (UNII: 4ELV7Z65AP) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:43074-112-11 3 g in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333B 06/10/2013 Labeler - Phillips Company (612368238) Establishment Name Address ID/FEI Business Operations Phillips Company 612368238 manufacture(43074-112)