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NDC 37808-0360-15 Hill Country Essentials Apricot Scrub Blemish and Blackhead Control 20 mg/g Details

Hill Country Essentials Apricot Scrub Blemish and Blackhead Control 20 mg/g

Hill Country Essentials Apricot Scrub Blemish and Blackhead Control is a TOPICAL EMULSION in the HUMAN OTC DRUG category. It is labeled and distributed by H.E.B.. The primary component is SALICYLIC ACID.

MedlinePlus Drug Summary

Topical salicylic acid is used to help clear and prevent pimples and skin blemishes in people who have acne. Topical salicylic acid is also used to treat skin conditions that involve scaling or overgrowth of skin cells such as psoriasis (a skin disease in which red, scaly patches form on some areas of the body), ichthyoses (inborn conditions that cause skin dryness and scaling), dandruff, corns, calluses, and warts on the hands or feet. Topical salicylic acid should not be used to treat genital warts, warts on the face, warts with hair growing from them, warts in the nose or mouth, moles, or birthmarks. Salicylic acid is in a class of medications called keratolytic agents. Topical salicylic acid treats acne by reducing swelling and redness and unplugging blocked skin pores to allow pimples to shrink. It treats other skin conditions by softening and loosening dry, scaly, or thickened skin so that it falls off or can be removed easily.

Related Packages: 37808-0360-15
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Salicylic Acid Topical

Product Information

NDC	37808-0360
Product ID	37808-360_e0566f40-9000-24d6-e053-2a95a90afed5
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Hill Country Essentials Apricot Scrub Blemish and Blackhead Control
Proprietary Name Suffix	n/a
Non-Proprietary Name	SALICYLIC ACID
Product Type	HUMAN OTC DRUG
Dosage Form	EMULSION
Route	TOPICAL
Active Ingredient Strength	20
Active Ingredient Units	mg/g
Substance Name	SALICYLIC ACID
Labeler Name	H.E.B.
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH FINAL
Application Number	part333D
Listing Certified Through	2024-12-31

Package

Package Images

NDC 37808-0360-15 (37808036015)

Pricing Information	N/A
NDC Package Code	37808-360-15
Billing NDC	37808036015
Package	170 g in 1 TUBE (37808-360-15)
Marketing Start Date	2010-11-11
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL e0566f35-8cef-f78e-e053-2a95a90a2ea7 Details

Active ingredient

Salicylic Acid 2.0%

Purpose

Acne Treatment

Uses

for the treatment of acne

Warnings

For external use only

When using this product

keep out of eyes. If contact occurs, immediately flush with water. • using other topical acne drugs at the same time or right after use of this product may increase dryness or irritation of the skin. If this occurs, only one drug should be used unless directed by a doctor.

Keep out of reach of children.

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

Directions

moisten face
apply with wet fingertips and massage into skin for about one minute
rinse well and pat dry

Other information

•store at room temperature •may stain or damage some fabrics, materials, or surfaces

Inactive ingredients

Water, Juglans Regia (Walnut) Shell Powder, Glyceryl Stearate SE, Propylene Glycol, Sodium Laureth Sulfate, Zea Mays (Corn) Kernel Meal, Cocamidopropyl Betaine, Cetearyl Alcohol, Triethanolamine, Cetyl Alcohol, PEG-100 Stearate, Glyceryl Stearate, Cetyl Acetate, Phenoxyethanol, Ceteareth-20, Titanium Dioxide, Polysorbate 60, Carbomer, Acetylated Lanolin Alcohol, Methylparaben, Ethylparaben, Fragrance (Parfum), Propylparaben, Limonene, Linalool, Hexyl Cinnamal, Benzyl Salicylate, Coumarin, Sorbitol, Butylphenyl Methylpropional, Geraniol, Salix Alba (Willow) Bark Extract, Sambucus Nigra Flower Extract, Primula Veris Extract, Helianthus Annuus (Sunflower) Extract, Chamomilla Recutita (Matricaria) Flower Extract, Glycerin, Prunus Armeniaca (Apricot) Fruit Extract

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HILL COUNTRY ESSENTIALS APRICOT SCRUB BLEMISH AND BLACKHEAD CONTROL

salicylic acid emulsion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:37808-360
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	20 mg in 1 g

Ingredient Name	Strength
Inactive Ingredients
BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)
HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)
CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)
WILLOW BARK (UNII: S883J9JDYX)
PRIMULA VERIS (UNII: W6LFQ57E4M)
COUMARIN (UNII: A4VZ22K1WT)
SORBITOL (UNII: 506T60A25R)
GERANIOL (UNII: L837108USY)
.ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
CORN GRAIN (UNII: C1Z9U7094Z)
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
CETYL ALCOHOL (UNII: 936JST6JCN)
GLYCERYL STEARATE/PEG-100 STEARATE (UNII: RD25J5V947)
ACETYLATED LANOLIN ALCOHOLS (UNII: SNN716810P)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
APRICOT (UNII: 269CJD5GZ9)
LIMONENE, (+/-)- (UNII: 9MC3I34447)
WATER (UNII: 059QF0KO0R)
CARBOMER HOMOPOLYMER TYPE B (ALLYL SUCROSE CROSSLINKED) (UNII: Z135WT9208)
JUGLANS REGIA SHELL (UNII: PJ10MT7VKA)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
CETYL ACETATE (UNII: 4Q43814HXS)
POLYSORBATE 60 (UNII: CAL22UVI4M)
TROLAMINE (UNII: 9O3K93S3TK)
ETHYLPARABEN (UNII: 14255EXE39)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
EUROPEAN ELDERBERRY JUICE (UNII: Z4IFJ0AK1E)
BENZYL SALICYLATE (UNII: WAO5MNK9TU)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:37808-360-15	170 g in 1 TUBE; Type 0: Not a Combination Product	11/11/2010

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part333D	11/11/2010

Labeler - H.E.B. (007924756)

Revised: 5/2022

Document Id: e0566f40-9000-24d6-e053-2a95a90afed5

Set id: e0566f35-8cef-f78e-e053-2a95a90a2ea7

Version: 1

Effective Time: 20220531