V RELIEF SERUM- dimethicone gel

V Relief Serum by

Drug Labeling and Warnings

V Relief Serum by is a Otc medication manufactured, distributed, or labeled by Kindra. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

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, Hydroxypropyl Starch Phosphate, Propanediol, Glycerin, Butyrospermum Parkii (Shea) Butter, Lactic Acid, Sodium Benzoate, Potassium Sorbate, Hydrogenated Lecithin, Akebia Quinata Extract, Sodium Hyaluronate, Phenethyl Alcohol, Ethylhexylglycerin, Maltodextrin, Pentapeptide-59, Tocopheryl Acetate (Vitamin E), Cocos Nucifera (Coconut) Oil

Questions?

310-906-0242

hello@ourkindra.com

DISTR. BY KINDRA

SANTA MONICA, CA 90404

Made in USA with US & imported materials

PRINCIPAL DISPLAY PANAL

KINDRA

V Relief Serum

Soothe and protect irritated vulvovaginal skin

ESTROGEN-FREE

PATENT-PENDING FORMULA:

• Skin-calming peptide
• Hyaluronic acid
• Vitamin E

Skin Protectant

NET WT 1.0 OZ (28g)

INGREDIENTS AND APPEARANCE

V RELIEF SERUM 
dimethicone gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84528-682
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
SHEA BUTTER (UNII: K49155WL9Y)
LACTIC ACID (UNII: 33X04XA5AT)
SODIUM BENZOATE (UNII: OJ245FE5EU)
HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)
PROPANEDIOL (UNII: 5965N8W85T)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
COCONUT OIL (UNII: Q9L0O73W7L)
PENTAPEPTIDE-59 (UNII: D8G3WTU93Z)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84528-682-30	1 in 1 BOX	09/01/2024
1		28 g in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product
2	NDC: 84528-682-75	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)