DAILY MOISTURIZER- lotion lotion

Daily Moisturizer by

Drug Labeling and Warnings

Daily Moisturizer by is a Otc medication manufactured, distributed, or labeled by Walgreens, APOLLO HEALTH AND BEAUTY CARE. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Dimethicone 1.2%

Purpose

Skin Protectant

Uses

• Helps prevent and temporarily protects chafted, chapped or cracked skin.
• Helps protect from the drying effects of wind and cold weather.

Warnings

For external use only.

When using this product

• do not get into eyes

Stop use and ask a doctor if

• Condition worsens
• Symptoms lasts more than 7 days or clear up and occur again with a few days.

Do not use on

• Deep or puncture wounds
• animal bites
• serious burns

Keep out of reach of children

If swallowed, get medical help or contact Poison Control Center right away.

Directions

Apply as needed.

Inactive Ingredients

Water (Aqua), Glycerin, Petrolatum, Isopropyl Palmatate, Distearyldimonium Chloride, Cetyl Alcohol, Avena Sativa (oat) kernel flour, Sodium Chloride, Sodium Hydroxide, Ethylhexylglycerin, Phenoxyethanol.

Questions or Comments?

1-800-925-4733.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DAILY MOISTURIZER 
lotion lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-5934
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O)	DIMETHICONE	1.2 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
CETYL ALCOHOL (UNII: 936JST6JCN)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
PETROLATUM (UNII: 4T6H12BN9U)
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)
OATMEAL (UNII: 8PI54V663Y)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-5934-02	71 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/19/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	12/19/2023

Labeler - Walgreens (008965063)

Registrant - APOLLO HEALTH AND BEAUTY CARE (201901209)

Establishment
Name	Address	ID/FEI	Business Operations
APOLLO HEALTH AND BEAUTY CARE		201901209	manufacture(0363-5934)