Label: TRACYS DOG PERSONAL LUBRICANT 300ML- personal lubricant oil
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Contains inactivated NDC Code(s)
NDC Code(s): 71352-0310-5 - Packager: Shenzhen Beston E-Commerce Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.
Drug Label Information
Updated December 5, 2018
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active ingredient
- Inactive ingredient
- Purpose
- When using
- Do not use
- Stop use
- Ask doctor
- Ask doctor/pharmacist
- Keep out of reach of children
- Questions
- Pregnancy or breast feeding
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Indications & usage
This product is a water-based personal lubricant, for penile and/or vaginal application, intended to lubricate and moisturize, to enhance the ease and comfort of intimate sexual activity and supplement to the body's natural lubricant.
Apply a small amount to genital areas. Reapply as needed or desired.
- Dosage & administration
- Dosage forms & strengths
- Warnings
- Package label. Principal display panel
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INGREDIENTS AND APPEARANCE
TRACYS DOG PERSONAL LUBRICANT 300ML
personal lubricant oilProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71352-0310 Route of Administration CUTANEOUS, EXTRACORPOREAL, VAGINAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN 48 g in 240 mL Inactive Ingredients Ingredient Name Strength HYDROXYETHYL CELLULOSE (1500 MPA.S AT 1%) (UNII: L605B5892V) 3.84 mL in 240 mL WATER (UNII: 059QF0KO0R) 186.048 mL in 240 mL SODIUM LACTATE (UNII: TU7HW0W0QT) 0.72 mL in 240 mL HYALURONIC ACID (UNII: S270N0TRQY) 0.72 mL in 240 mL BENZOIC ACID (UNII: 8SKN0B0MIM) 0.192 mL in 240 mL LACTIC ACID, DL- (UNII: 3B8D35Y7S4) 0.48 mL in 240 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71352-0310-5 240 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/05/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 12/05/2018 Labeler - Shenzhen Beston E-Commerce Co., Ltd. (544481234) Registrant - A03 Lab of BTS (548009541) Establishment Name Address ID/FEI Business Operations Shenzhen Beston E-Commerce Co., Ltd. 544481234 label(71352-0310) , manufacture(71352-0310)