HEB MAXIMUM STRENGTH PAIN RELIEF HEMORRHOIDAL- glycerin, petrolatum, phenylephrine hydrochloride, and pramoxine hydrochloride cream

HEB Maximum Strength Pain Relief Hemorrhoidal by

Drug Labeling and Warnings

HEB Maximum Strength Pain Relief Hemorrhoidal by is a Otc medication manufactured, distributed, or labeled by HEB, Natureplex LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

Active ingredients	Purposes
Glycerin 14.4%	Protectant
Petrolatum 15%	Protectant
Phenylephrine hydrochloride 0.25%	Vasoconstrictor
Pramoxine hydrochloride 1%	Local Anesthetic

Uses

• temporarily relieves pain, soreness, and burning
• helps relieve local itching and discomfort associated with hemorrhoids
• temporarily shrinks hemorrhoidal tissue
• temporarily provides a coating for relief of anorectal discomforts
• temporarily protects the inflamed, irritated anorectal surface to help make bowel movements less painful

Warnings

For external use only.

Ask a doctor before use if you have

• heart disease
• high blood pressure
• thyroid disease
• diabetes
• difficulty urinating due to enlargement of the prostate gland

Ask a doctor or pharmacist before use if you are taking a prescription drug for high blood pressure or depression

When using this product

• do not exceed the recommended daily dosage unless directed by a doctor
• do not put into rectum by using fingers or any mechanical device or applicator

Stop use and ask a physician if

• bleeding occurs
• the condition worsens or does not improve within 7 days
• an allergic reaction develops
• the symptom being treated does not subside or redness, irritation, swelling, pain, or other symptoms develops, persists, or increase

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away: 800-222-1222.

Directions

Adults:

• when practical, cleanse affected area by patting or blotting with appropriate cleansing wipe. Gently dry by patting or blotting with tissue or soft cloth before applying cream.
• when first opening tube, remove foil seal
• apply externally or in lower portion of anal canal only
• apply externally to affected area up to 4 times daily, especially at night, in the morning, or after each bowel movement
• for application in lower anal canal; remove cover from dispensing cap. Attach dispensing cap to tube. Lubriate dispensing cap well, then gently insert dispensing cap partway into anus
• thoroughly cleanse dispensing cap after each use, and replace cover
• Children under 12 years: ask a doctor

Other information

• store at 15 to 30°C (59 to 86°F).
• close cap tightly after use
• Tamper Evident: DO NOT USE IF SEAL ON TUBE IS PUNCTURED OR MISSING.

Inactive ingredients

aloe barbadensis leaf juice, BHA, cetyl alcohol, citric acid, disodium EDTA, glyceryl stearate, laureth-23, methylparaben, mineral oil, panthenol, propyl gallate, propylene glycol, propylparaben, purified water, sodium benzoate, sodium carboxymethylcellulose, steareth-2, steareth-20, stearyl alcohol, tocopherol (vitamin E) acetate, xanthan gum

Questions or comments?

866-323-0107

PRINCIPAL DISPLAY PANEL - 56.7 g Tube Carton

Compare to Preperation H® Cream active ingredients*

NDC: 37808-992-24

H-E-B®

Maximum Strength Pain Relief
Hemorrhoidal Cream
Phenylephrine Hydrochloride / Vasoconstrictor Pramoxine Hydrochloride / Local Anesthetic

Hemorrhoid Symptom Relief

With Soothing Aloe
Rapid, Soothing Pain Relief from Painful Burning, Itching and Discomfort
Shrinks Swollen Hemorrhoidal Tissue Protects Irritated Tissue
Relieves External Discomfort

Includes
Dispensing
Cap

NET WT 2.0 OZ (56.7 g)

INGREDIENTS AND APPEARANCE

HEB MAXIMUM STRENGTH PAIN RELIEF HEMORRHOIDAL 
glycerin, petrolatum, phenylephrine hydrochloride, and pramoxine hydrochloride cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 37808-992
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	0.144 mg  in 2 g
PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U)	PETROLATUM	0.15 mg  in 2 g
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV)	PHENYLEPHRINE HYDROCHLORIDE	0.0025 mg  in 2 g
PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056)	PRAMOXINE HYDROCHLORIDE	0.1 mg  in 2 g

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)
CETYL ALCOHOL (UNII: 936JST6JCN)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
EDETATE DISODIUM (UNII: 7FLD91C86K)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
LAURETH-23 (UNII: N72LMW566G)
METHYLPARABEN (UNII: A2I8C7HI9T)
MINERAL OIL (UNII: T5L8T28FGP)
PANTHENOL (UNII: WV9CM0O67Z)
PROPYL GALLATE (UNII: 8D4SNN7V92)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
WATER (UNII: 059QF0KO0R)
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)
STEARETH-2 (UNII: V56DFE46J5)
STEARETH-20 (UNII: L0Q8IK9E08)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
XANTHAN GUM (UNII: TTV12P4NEE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 37808-992-24	1 in 1 CARTON	10/18/2018
1		56.7 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part346	10/18/2018

Labeler - HEB (007924756)

Establishment
Name	Address	ID/FEI	Business Operations
Natureplex LLC		062808196	MANUFACTURE(37808-992)