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NDC 71505-0022-80 Honey Pot 10 mg/mL Details

Honey Pot 10 mg/mL

Honey Pot is a TOPICAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by Disposable Hygiene LLC dba Anthem. The primary component is PRAMOXINE HYDROCHLORIDE.

MedlinePlus Drug Summary

Pramoxine is used to temporarily relieve pain and itching from insect bites; poison ivy, poison oak, or poison sumac; minor cuts, scrapes, or burns; minor skin irritation or rashes; or dry, itchy skin. Pramoxine also may be used to treat soreness, burning, itching, and pain from hemorrhoids (''piles'') and other minor rectal irritations or itching. Pramoxine is in a class of medications called topical anesthetics. It works by stopping nerves from sending pain signals.

Related Packages: 71505-0022-80
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Pramoxine

Product Information

NDC	71505-0022
Product ID	71505-022_ddc4f5ad-9ed8-cc1a-e053-2a95a90a8668
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	Honey Pot
Proprietary Name Suffix	n/a
Non-Proprietary Name	Anti-Itch Soothing
Product Type	HUMAN OTC DRUG
Dosage Form	LIQUID
Route	TOPICAL
Active Ingredient Strength	10
Active Ingredient Units	mg/mL
Substance Name	PRAMOXINE HYDROCHLORIDE
Labeler Name	Disposable Hygiene LLC dba Anthem
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH NOT FINAL
Application Number	part348
Listing Certified Through	2023-12-31

Package

Package Images

NDC 71505-0022-80 (71505002280)

Pricing Information	N/A
NDC Package Code	71505-022-80
Billing NDC	71505002280
Package	80 mL in 1 BOTTLE (71505-022-80)
Marketing Start Date	2022-02-15
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL ddc4f5ad-9ed9-cc1a-e053-2a95a90a8668 Details

Active Ingredient(s)

Pramoxine hydrochloride 1% (w/w)

Purpose

External analgesic

Use

For temporary relief of pain and itching associated with minor skin irritations.

Warnings

For external use only.

SPL UNCLASSIFIED SECTION

When using this product: avoid contact with eyes.

SPL UNCLASSIFIED SECTION

Stop use and ask a doctor if: • Condition worsens • If symptoms persist for more than 7 days, or clear up and reoccur again within a few days.

SPL UNCLASSIFIED SECTION

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

Directions

Adults and children 12 years of age and older: Apply to the affected area not more than 3 or 4 times daily. Children under 12 years of age: Consult a doctor

Inactive ingredients

Water, Polysorbate 20, Glycerin, Pentylene Glycol, Hamamelis virginiana (Witch Hazel) Water, Benzoic Acid, Fragrance, Honey, Vinegar, Aloe Barbadensis Leaf Juice, Sodium Hydroxide, Cucumis Sativus (Cucumber) Fruit Extract, Lavender (Lavandula Angustifolia) Extract, Calendula Officinalis (Calendula) Flower Extract, Cocos Nucifera (Coconut) Fruit Extract, Allium Sativum (Garlic) Extract, Olea Europaea (Olive) Leaf Extract, Potassium Sorbate, Sodium Benzoate, Citric Acid

Other information

Store at a controlled room temperature of 77°F (20-25°C).

SPL UNCLASSIFIED SECTION

For questions and general information visit us at www.thehoneypot.co/contact

Package Label - Principal Display Panel

80 mL NDC: 71505-022-80

INGREDIENTS AND APPEARANCE

HONEY POT

anti-itch soothing liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:71505-022
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056)	PRAMOXINE HYDROCHLORIDE	10 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
ACETIC ACID (UNII: Q40Q9N063P)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
LAVENDER OIL (UNII: ZBP1YXW0H8)
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
GARLIC OIL (UNII: 4WG8U28833)
OLEA EUROPAEA LEAF (UNII: MJ95C3OH47)
SODIUM BENZOATE (UNII: OJ245FE5EU)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
GLYCERIN (UNII: PDC6A3C0OX)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
WATER (UNII: 059QF0KO0R)
BENZOIC ACID (UNII: 8SKN0B0MIM)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WITCH HAZEL (UNII: 101I4J0U34)
HONEY (UNII: Y9H1V576FH)
CUCUMBER FRUIT OIL (UNII: R81Y52NPCT)
COCONUT OIL (UNII: Q9L0O73W7L)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:71505-022-80	80 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/15/2022

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part348	02/15/2022

Labeler - Disposable Hygiene LLC dba Anthem (079848737)

Name	Address	ID/FEI	Business Operations
Establishment
Disposable Hygiene LLC dba Anthem		079848737	manufacture(71505-022)

Revised: 2/2022

Document Id: ddc4f5ad-9ed8-cc1a-e053-2a95a90a8668

Set id: ddc4f5ad-9ed9-cc1a-e053-2a95a90a8668

Version: 1

Effective Time: 20220215

Search by Drug Name or NDC

NDC 71505-0022-80 Honey Pot 10 mg/mL Details

Honey Pot 10 mg/mL

MedlinePlus Drug Summary

Product Information

Package

Package Images

NDC 71505-0022-80 (71505002280)

Contents

Standard Product Labeling (SPL)/Prescribing Information SPL ddc4f5ad-9ed9-cc1a-e053-2a95a90a8668 Details

Active Ingredient(s)

Purpose

Use

Warnings

SPL UNCLASSIFIED SECTION

SPL UNCLASSIFIED SECTION

SPL UNCLASSIFIED SECTION

Directions

Inactive ingredients

Other information

SPL UNCLASSIFIED SECTION

Package Label - Principal Display Panel

INGREDIENTS AND APPEARANCE

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