Label: UTIMI WATER BASED PERSONAL LUBRICANT- personal lubricant lotion
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Contains inactivated NDC Code(s)
NDC Code(s): 82624-101-03 - Packager: Shenzhen Guangdian Technology Co., Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated March 19, 2022
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- Official Label (Printer Friendly)
- Active ingredient
- Inactive ingredient
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Indication for use
Utimi Personal Lubricant is a water-based lubricant for penile or vaginal application, intended to moisturize and enhance the ease and comfort of intimate sexual activity as well as supplement for the body's natural lubrication.
This product is compatible with natural rubber latex, polyurethane and polyisoprene condoms.
- Do not use
- Stop use
- Ask doctor/physician
- Keep out of reach of children
- Questions
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Indications & usage
Utimi Personal Lubricant is a water-based lubricant for penile or vaginal application, intended to moisturize and enhance the ease and comfort of intimate sexual activity as well as supplement for the body's natural lubrication.
This product is compatible with natural rubber latex, polyurethane and polyisoprene condoms.
This product is not a contraceptive or spermicide.
- Direction
- Dosage forms & strengths
- Warnings
- Package label. Principal display panel
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INGREDIENTS AND APPEARANCE
UTIMI WATER BASED PERSONAL LUBRICANT
personal lubricant lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82624-101 Route of Administration VAGINAL, RECTAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HYDROXYETHYL CELLULOSE (140 CPS AT 5%) (UNII: 8136Y38GY5) (HYDROXYETHYL CELLULOSE (140 CPS AT 5%) - UNII:8136Y38GY5) HYDROXYETHYL CELLULOSE (140 CPS AT 5%) 393 mg in 30 mL Inactive Ingredients Ingredient Name Strength SODIUM BENZOATE (UNII: OJ245FE5EU) WATER (UNII: 059QF0KO0R) POLYSORBATE 20 (UNII: 7T1F30V5YH) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) LACTIC ACID, DL- (UNII: 3B8D35Y7S4) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82624-101-03 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/21/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 03/21/2022 Labeler - Shenzhen Guangdian Technology Co., Ltd (402547791) Establishment Name Address ID/FEI Business Operations Shenzhen Guangdian Technology Co., Ltd 402547791 manufacture(82624-101) , label(82624-101)
