HYDRATING MOISTURE DAY AND NIGHTCREAM- citronellol, geraniol cream

Hydrating moisture day and nightcream by

Drug Labeling and Warnings

Hydrating moisture day and nightcream by is a Otc medication manufactured, distributed, or labeled by inthismorning co ltd, cosmax inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

citronellol, geraniol

INACTIVE INGREDIENT

water, glycerin, etc

PURPOSE

moisturizing, whitening, wrinkle care

KEEP OUT OF REACH OF CHILDREN

keep out or reach of the children

INDICATIONS & USAGE

apply proper amount to the skin

WARNINGS

This product is for exeternal use only. Do not use for internal use
Storage and handling precautions
If possible, avoid direct sunlight and store in cool and area of low humidity in order to maintain the quality of the product and avoid misuse
Avoid placing the product near fire and store out in reach of children

- consult a physician in case of abnormal symptoms, such as red spots, swelling or itching, or side effects in the areas of application due to direct light during or after using the product

- do not use on wounded area

DOSAGE & ADMINISTRATION

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HYDRATING MOISTURE DAY AND NIGHTCREAM 
citronellol, geraniol cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71217-0071
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
.BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K) (.BETA.-CITRONELLOL, (R)- - UNII:P01OUT964K)	.BETA.-CITRONELLOL, (R)-	0.0090402 g  in 100 mL
GERANIOL (UNII: L837108USY) (GERANIOL - UNII:L837108USY)	GERANIOL	0.003019275 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71217-0071-1	15 mL in 1 TUBE; Type 0: Not a Combination Product	01/15/2023
2	NDC: 71217-0071-2	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/15/2023
3	NDC: 71217-0071-3	120 mL in 1 TUBE; Type 0: Not a Combination Product	01/15/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		01/15/2023

Labeler - inthismorning co ltd (695126076)

Registrant - inthismorning co ltd (695126076)

Establishment
Name	Address	ID/FEI	Business Operations
cosmax inc		689049693	manufacture(71217-0071)

Establishment
Name	Address	ID/FEI	Business Operations
inthismorning co ltd		695126076	label(71217-0071)