BABY OIL- glycerin oil solution

Baby Oil by

Drug Labeling and Warnings

Baby Oil by is a Otc medication manufactured, distributed, or labeled by NANONATURE. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Glycerin (11.0%) - Skin Protectant

INACTIVE INGREDIENT

Water, Olive Oil, Lemon Balm Extract, Ginseng Extract, Chinese Matrimony Vine Extract, Ethanol, N-acetyl Glucosamine, Menthol, Collagen, Aromatic, Retinol, Ascorbic Acid, Tocopherol

PURPOSE

Skin Protectant

WARNINGS

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 baby’s face and body
 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 baby’s face and body
 Frequency of usage should accord to skin condition

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BABY OIL 
glycerin oil solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71538-006
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Glycerin (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	Glycerin	11 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Olive Oil (UNII: 6UYK2W1W1E)
Retinol (UNII: G2SH0XKK91)
Tocopherol (UNII: R0ZB2556P8)
Ascorbic Acid (UNII: PQ6CK8PD0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71538-006-01	100 mL in 1 PACKAGE; Type 0: Not a Combination Product	07/17/2017

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	Business Operations
NANONATURE		689851291	manufacture(71538-006)