DAILY VLOTION- dimethicone lotion

Daily VLotion by

Drug Labeling and Warnings

Daily VLotion by is a Otc medication manufactured, distributed, or labeled by Kindra. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Dimethicone 2%

Purpose

Skin Protectant

Use

• helps prevent, temporarily protects, and helps relieve chafed, chapped, or cracked skin

Warnings

For external use only

When using this product do not get into eyes

Stop use and ask a doctor if

• condition worsens
• symptoms last more than 7 days or clear up and occur again within a few days

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

Directions

apply generously as needed

Inactive ingredients

Water, Glycerin, Cetearyl Alcohol, Helianthus Annuus (Sunflower) Seed Oil, Cetyl Alcohol, Coco-Glucoside, Butyrospermum Parkii (Shea) Butter, Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Sodium Hyaluronate, C15-19 Alkane, Glyceryl Stearate Citrate, Cocos Nucifera (Coconut) Oil, Lactic Acid, Bisabolol, Tocopherol, Sodium Benzoate, Potassium Sorbate, Hydrogenated Lecithin, Polyglyceryl-6 Laurate, Phenethyl Alcohol, Ethylhexylglycerin, Polyglycerin-6, Maltodextrin, Pentapeptide-59

Questions?

310-906-0242

hello@ourkindra.com

DISTR BY KINDRA

SANTA MONICA, CA 90404

Made in USA with US & imported materials

PRINCIPAL DISPLAY PANEL

KINDRA

Daily V Lotion

Hydrate and protect dry vulvovaginal skin

ESTROGEN-FREE

PATENT-PENDING FORMULA:

• Skin-calming peptide
• Shea butter
• Coconut oil

Skin Protectant

NET WT 1.0 OZ (28g)

INGREDIENTS AND APPEARANCE

DAILY VLOTION 
dimethicone lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84528-359
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O)	DIMETHICONE	0.56 g  in 28 g

Inactive Ingredients
Ingredient Name	Strength
COCONUT OIL (UNII: Q9L0O73W7L)
LACTIC ACID (UNII: 33X04XA5AT)
WATER (UNII: 059QF0KO0R)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
SUNFLOWER OIL (UNII: 3W1JG795YI)
CETYL ALCOHOL (UNII: 936JST6JCN)
SHEA BUTTER (UNII: K49155WL9Y)
SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
GLYCERYL STEARATE CITRATE (UNII: WH8T92A065)
GLYCERIN (UNII: PDC6A3C0OX)
LEVOMENOL (UNII: 24WE03BX2T)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
TOCOPHEROL (UNII: R0ZB2556P8)
C15-19 ALKANE (UNII: CI87N1IM01)
POLYGLYCERIN-6 (UNII: M51422LRAM)
COCO-GLUCOSIDE (UNII: ICS790225B)
SODIUM BENZOATE (UNII: OJ245FE5EU)
POLYGLYCERYL-6 LAURATE (UNII: Q48X4BL3TV)
PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84528-359-30	1 in 1 BOX	09/01/2024
1		28 g in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product
2	NDC: 84528-359-75	1 in 1 BOX	09/01/2024
2		70 g in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	09/01/2024

Labeler - Kindra (118193128)