Label: VITA-P ORAL AND NASAL- menthol 1% aerosol, spray
- NDC Code(s): 71073-308-01
- Packager: Beijing HKKY Medical Tech. Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not 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 August 13, 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 Ingredients
- Purpose
- Uses
- Warnings
- Do Not Use
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When Using This Product
Use it with caution for minors
Stop use and seek medical treatment if discomfort during use
·People over 65 years old, asthma patients, heart disease patients, pregnant women use with caution
·Disabled under the age of 12
·This product is for single person use, shall not cross use
Use of this container by more than one person may spread infection - PREGNANCY OR BREAST FEEDING
- Keep Out of Reach of Children
- Other information
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Directions
Model and specification: 2 ml nano-aerosol
·This product is composed of menthol and dihydroquercetin solution and oral inhaler, non-sterile product use·Use method: ① Open the bottle cap ② remove silicone nail ③ oral inhalation ④one inhaling last 3 seconds
·The thermal sensation should be automatically atomized, and when the mouth is contained,
it can be inhaled immediately, for 3 seconds at once a time,
It is recommended to do this 3-5 times per day in the morning, afternoon and evening.
·Packaging is damaged, do not use it - Inactive Ingredients
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
VITA-P ORAL AND NASAL
menthol 1% aerosol, sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71073-308 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 0.01 g in 1 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) DIHYDROQUERCETIN GLUCOSIDE (UNII: 6H7474G841) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71073-308-01 2 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 08/13/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 08/11/2023 Labeler - Beijing HKKY Medical Tech. Co., Ltd. (544434817) Establishment Name Address ID/FEI Business Operations Beijing HKKY Medical Tech. Co., Ltd. 544434817 manufacture(71073-308)