Label: VIABECLINE FIRST AID ANTIBIOTIC- tetracycline hydrochloride ointment
- NDC Code(s): 69006-005-00, 69006-005-01
- Packager: VIADERMA II, INC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 30, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient (in each gram)
- Use
- Warnings
- Directions
-
Other information
- Keep product refrigerated to pressrve 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.
- Containa 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
- Package Labeling:
-
INGREDIENTS AND APPEARANCE
VIABECLINE FIRST AID ANTIBIOTIC
tetracycline hydrochloride ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69006-005 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 mL Inactive Ingredients Ingredient Name Strength ACETIC ACID (UNII: Q40Q9N063P) 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) HISTIDINE (UNII: 4QD397987E) 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:69006-005-00 1 in 1 BOX 05/13/2017 1 15 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:69006-005-01 28 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/13/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M004 05/13/2017 Labeler - VIADERMA II, INC. (079387584)