Dimethicone by H E B / Vi-Jon, LLC DIMETHICONE lotion

Dimethicone by

Drug Labeling and Warnings

Dimethicone by is a Otc medication manufactured, distributed, or labeled by H E B, Vi-Jon, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Dimethicone 1.2%

Purpose

Skin protectant

Uses

• helps prevent and temporarily protects chapped or cracked skin
• helps protect from the drying effects of wind and cold weather

Warnings

For external use only

Do not use on

• deep or puncture wounds
• animal bites
• serious burns

When using this product

do not get into eyes

Stop use and ask a doctor if

• condition worsens
• symptoms last more then 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 Poison Control right away.

Directions 

• apply as needed

Other information

store between 15°-30°C (59°-86°F)

inactive ingredients

water, glycerin, distearyldimonium chloride, petrolatum, isopropyl palmitate, cetyl alcohol, Avena sativa (oat) kernel flour, benzyl alcohol, sodium chloride, sodium hydroxide

ADVERSE REACTION

DISTRIBUTED BY: H-E-B ®, SAN ANTONIO, TN 78204

LOT NUMBER: ON PACKAGE 

QUESTIONS OR COMMENTS?

CALL TOLL FREE 1-888-593-0593

We hope you are satisfied with this product. 

If not, we will cheerfully refund your money.

Principal panel display

HILL COUNTRY FARE ®

Baby Lotion

WITH COLLOIDAL OATMEAL

SKIN PROTECTANT

Hypoallergenic

Fragrance Free

Free From

• Parabens
• Phthalates
• Dyes

NET WT 8 OZ

CONT. NET. 227 g

INGREDIENTS AND APPEARANCE

DIMETHICONE 
dimethicone lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 37808-496
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O)	DIMETHICONE	12 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)
PETROLATUM (UNII: 4T6H12BN9U)
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
CETYL ALCOHOL (UNII: 936JST6JCN)
OATMEAL (UNII: 8PI54V663Y)
BENZYL ALCOHOL (UNII: LKG8494WBH)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 37808-496-34	227 g in 1 TUBE; Type 0: Not a Combination Product	06/05/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	06/05/2023

Labeler - H E B (007924756)

Registrant - Nice-Pak Products, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Nice-Pak Products, LLC		119091514	manufacture(37808-496)