Label: AOPAR WATER BASED PERSONAL LUBRICANT- personal lubricant lotion
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Contains inactivated NDC Code(s)
NDC Code(s): 73000-226-20 - Packager: Shenzhen ZhiHuiChuangXiang Technology 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 April 13, 2021
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- Active ingredient
- Inactive ingredient
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Indications & usage
Aopar Water-based Personal Lubricant is a supplement for the nature lubrication of penis or vagina, intending to moisturize and enhance the ease and comfort of intimate sexual activity.
This product is compatible with natural rubber latex, polyurethane and polyisoprene condoms.
This product is not a contraceptive or spermicide.
- Direction
- Dosage forms & strengths
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- Package label. Principal display panel
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INGREDIENTS AND APPEARANCE
AOPAR WATER BASED PERSONAL LUBRICANT
personal lubricant lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73000-226 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%) 0.381 g in 30 mL Inactive Ingredients Ingredient Name Strength SODIUM BENZOATE (UNII: OJ245FE5EU) 0.3 mL in 30 mL WATER (UNII: 059QF0KO0R) 25.008 mL in 30 mL POLYSORBATE 20 (UNII: 7T1F30V5YH) 0.075 mL in 30 mL GLYCERIN (UNII: PDC6A3C0OX) 2.538 mL in 30 mL PROPYLENE GLYCOL (UNII: 6DC9Q167V3) 1.665 mL in 30 mL LACTIC ACID, DL- (UNII: 3B8D35Y7S4) 0.006 mL in 30 mL EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) 0.027 mL in 30 mL Product Characteristics Color white Score no score Shape FREEFORM Size 50mm Flavor MINT Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73000-226-20 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/13/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 04/13/2021 Labeler - Shenzhen ZhiHuiChuangXiang Technology Co., Ltd (550748186) Registrant - Shenzhen ZhiHuiChuangXiang Technology Co., Ltd (550748186) Establishment Name Address ID/FEI Business Operations Shenzhen ZhiHuiChuangXiang Technology Co., Ltd 550748186 manufacture(73000-226) , label(73000-226)
