OTC Medication Information: Ultra Moisturizing Essence

ULTRA MOISTURIZING ESSENCE- glycerin solution
NANONATURE

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.

ACTIVE INGREDIENT

Glycerin (12.3%) — Skin Protectant

INACTIVE INGREDIENT

Water, Olein Acid, Lemon Balm Extract, Olive Oil, Angelica Gigas NAKAI Extract, Chinese Matrimony Vine Extract, Ginseng Extract, Retinol, Tocopherol, Ascobic Acid, Aromatic

PURPOSE

Skin Protectant

WARNINGS

For skin use only.
Do not use
 on puncture wounds  on animal bites
When using this product
 avoid contact with eyes
Stop use and ask a doctor if
 you have allergy or skin disease
 rash or irritation develops and lasts
 red spots, swelling, itching, irritation and other abnormalities developsFor skin use only.
Do not use
 on puncture wounds  on animal bites
When using this product
 avoid contact with eyes
Stop use and ask a doctor if
 you have allergy or skin disease
 rash or irritation develops and lasts
 red spots, swelling, itching, irritation and other abnormalities develops

KEEP OUT OF REACH OF CHILDREN

 if swallowed, get medical help or contact a Poison Control Center right away

INDICATIONS & USAGE

 Clean skin thoroughly before using
 Squeeze 1 or 2 pumps onto palm
 Apply lightly to a slightly wet face
 Frequency of usage should accord to skin condition

DOSAGE & ADMINISTRATION

 Clean skin thoroughly before using
 Squeeze 1 or 2 pumps onto palm
 Apply lightly to a slightly wet face Frequency of usage should accord to skin condition

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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ULTRA MOISTURIZING ESSENCE glycerin essence solution
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:71538-002
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Glycerin (GLYCERIN) Glycerin 12.3 g in 100 mL
Inactive Ingredients
Ingredient Name Strength
Water
Olive Oil
Tocopherol
Retinol
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:71538-002-01 100 mL in 1 PACKAGE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 07/17/2017
Labeler — NANONATURE (689851291)
Registrant — NANONATURE (689851291)
Establishment
Name Address ID/FEI Operations
NANONATURE 689851291 manufacture (71538-002)

Revised: 07/2017 NANONATURE

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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