IvyMed
- Manufacturer
- Phillips Company
- Effective date
- 2010-09-04
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 18
- Source
- full-release
- Hydrated at
- 2026-05-31 22:32:11
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
DRUG FACTS
Questions and Side effects
Use of this product results in no known side effects when used according to directions. Phillips Company, 311 Chickasaw Street, Millerton, OK USA 74750; Tel. 580-746-2430
Email address: hp@valliant.net
ACTIVE INGREDIENTS
Active Ingredients Purpose
Zinc acetate (.1% by volume) Skin Protectant
ASK DOCTOR
Ask a doctor
If symptoms last for more than 7 days or clear up and recur within a few days.
If the conditions do not improve.
Before use on children under 2 years.
Before use if you are allergic to any ingredients listed on this label.
DO NOT USE
Warnings
For external use only
Keep away from children
Avoid contact with eyes
May be harmful if swallowed or inhaled
CHILDREN
Keep away from children
Avoid contact with eyes
May be harmful if swallowed or inhaled
PURPOSE
Active Ingredients Purpose
Zinc acetate (.1% by volume) Skin Protectant
STOP USE
If symptoms last for more than 7 days or clear up and recur within a few days.
If the conditions do not improve.
Before use on children under 2 years.
Before use if you are allergic to any ingredients listed on this label.
WHEN USING
For external use only
Avoid contact with eyes
May be harmful if swallowed or inhaled
If symptoms last for more than 7 days or clear up and recur within a few days.
If the conditions do not improve.
Store at 40 to 120 degrees F.
WARNINGS
Warnings
For external use only
Keep away from children
Avoid contact with eyes
May be harmful if swallowed or inhaled
Use of this product results in no known side effects when used according to directions.
Phillips Company, 311 Chickasaw Street, Millerton, OK USA 74750; Tel. 580-746-2430
Email address: hp@valliant.net
DOSAGE & ADMINISTRATION
Uses
Temporarily protects injured or exposed skin or mucous membrane surfaces from harmful or annoying stimuli and may help provide relief to such surfaces
Directions
Apply to affected skin area and rub gently. Repeat the process as needed.
USE
Uses
Temporarily protects injured or exposed skin or mucous membrane surfaces from harmful or annoying stimuli and may help provide relief to such surfaces
Apply to affected skin area and rub gently. Repeat the process as needed.
INACTIVE INGREDIENTS
Inactive ingredients
Water, color, glycerin, hydroxethylcellulose, chlor-hexidine gluconate, glucono delta lactone, methylparaben, sodium hydroxide,sodium dodecylbenzene sulfonate, dimethyl sulfoxide, witch hazel, ascorbic acid, magnesium stearate, silica and stearic acid.
Image of product
Image of product
DailyMed RxNorm Mappings#
DailyMed Pharmacologic Classes#
| Class | Version | Type | Effective |
|---|---|---|---|
| ZINC CATION Pharmacologic Class Indexing | 2 | Indexing - Pharmacologic Class | 20180813 |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| f47a510b-6679-4664-b2d6-47b5c4afe7cc | Product name | 4 | 20260217 |
| bee4fa8d-8d82-423a-a0b5-40a89dd13a99 | Product name | 1 | 20250618 |
| 030ce964-9b2d-45aa-b5d3-f78ce03ef61c | Product name | 2 | 20250515 |
| 6c13b22c-b3ba-4127-b768-0132dd5ab0d1 | Product name | 1 | 20230829 |
| 0306390c-dd77-4363-afe0-63c58088b2a1 | Product name | 1 | 20220120 |
| 503ea967-4b9c-48cf-9e87-c7975295849d | Product name | 2 | 20220120 |
| c5cd4727-ac49-4409-82b1-5bd8006c3ec7 | Product name | 1 | 20171122 |
| bb6d6c68-649d-4e6d-a1f6-603d969c8f68 | Product name | 1 | 20160303 |
| 190f2a5b-bbc8-65c7-fcb0-97891307b917 | Product name | 1 | 20140508 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 43074-208-02 | 2019-11-13 | C162847 | 48780-1 | 97449f38-c27b-f6ea-e053-dbdaa90aa703 | DRUG FACTS |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 43074-208-01 | IvyMed | 3 mL in 1 BOTTLE, DROPPER | LIQUID | 3 | 18 | |
| 43074-208-02 | IvyMed | 1 in 1 BOTTLE, PLASTIC | LIQUID | 1 | 18 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| ZINC ACETATE | ACTIVE INGREDIENT | FM5526K07A | 18 | |
| ZINC CATION | ACTIVE MOIETY | 13S1S8SF37 | 18 | |
| ascorbic acid | INACTIVE INGREDIENT | PQ6CK8PD0R | 18 | |
| calcium gluconate | INACTIVE INGREDIENT | SQE6VB453K | 18 | |
| chlorhexidine gluconate | INACTIVE INGREDIENT | MOR84MUD8E | 18 | |
| dimethyl sulfoxide | INACTIVE INGREDIENT | YOW8V9698H | 18 | |
| dipropylene glycol | INACTIVE INGREDIENT | E107L85C40 | 18 | |
| glycerin | INACTIVE INGREDIENT | PDC6A3C0OX | 18 | |
| magnesium stearate | INACTIVE INGREDIENT | 70097M6I30 | 18 | |
| methylparaben | INACTIVE INGREDIENT | A2I8C7HI9T | 18 | |
| sodium dodecylbenzenesulfonate | INACTIVE INGREDIENT | 554127163Y | 18 | |
| sodium hydroxide | INACTIVE INGREDIENT | 55X04QC32I | 18 | |
| sorbic acid | INACTIVE INGREDIENT | X045WJ989B | 18 | |
| stearic acid | INACTIVE INGREDIENT | 4ELV7Z65AP | 18 | |
| water | INACTIVE INGREDIENT | 059QF0KO0R | 18 | |
| witch hazel | INACTIVE INGREDIENT | 101I4J0U34 | 18 |
Products#
Every source-derived product name is available through these pages.
- IvyMed
- zinc acetate
- ZINC CATION
- dimethyl sulfoxide
- ascorbic acid
- dipropylene glycol
- water
- glycerin
- chlorhexidine gluconate
- calcium gluconate
- methylparaben
- sodium hydroxide
- sorbic acid
- magnesium stearate
- stearic acid
- witch hazel
- sodium dodecylbenzenesulfonate
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 43074-208 | 43074-208-01, 43074-208-02 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ZINC ACETATE | FM5526K07A | ACTIM |
| dimethyl sulfoxide | YOW8V9698H | IACT |
| ascorbic acid | PQ6CK8PD0R | IACT |
| dipropylene glycol | E107L85C40 | IACT |
| water | 059QF0KO0R | IACT |
| glycerin | PDC6A3C0OX | IACT |
| chlorhexidine gluconate | MOR84MUD8E | IACT |
| calcium gluconate | SQE6VB453K | IACT |
| methylparaben | A2I8C7HI9T | IACT |
| sodium hydroxide | 55X04QC32I | IACT |
| sorbic acid | X045WJ989B | IACT |
| magnesium stearate | 70097M6I30 | IACT |
| stearic acid | 4ELV7Z65AP | IACT |
| witch hazel | 101I4J0U34 | IACT |
| sodium dodecylbenzenesulfonate | 554127163Y | IACT |
Source Document#
Inactive ingredient matches#
Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| sodium hydroxide | SODIUM HYDROXIDE | 55X04QC32I | SOLUTION / SUBCUTANEOUS | ADJ PH | ||
| sodium hydroxide | SODIUM HYDROXIDE | 55X04QC32I | INJECTION / PERIDURAL | ADJ PH | ||
| stearic acid | STEARIC ACID | 4ELV7Z65AP | LOTION / TOPICAL | 80 mg | ||
| magnesium stearate | MAGNESIUM STEARATE | 70097M6I30 | SUSPENSION, EXTENDED RELEASE / ORAL | 71 mg | ||
| sodium hydroxide | SODIUM HYDROXIDE | 55X04QC32I | ELIXIR / ORAL | ADJ PH | ||
| stearic acid | STEARIC ACID | 4ELV7Z65AP | AEROSOL, FOAM / VAGINAL | 4 %w/w | ||
| sodium hydroxide | SODIUM HYDROXIDE | 55X04QC32I | INJECTION / DENTAL | ADJ PH | ||
| stearic acid | STEARIC ACID | 4ELV7Z65AP | OINTMENT / TOPICAL | 15 %w/w | ||
| methylparaben | METHYLPARABEN | A2I8C7HI9T | DROPS / AURICULAR (OTIC) | 0.01 %w/w | ||
| methylparaben | METHYLPARABEN | A2I8C7HI9T | FILM, SOLUBLE / BUCCAL | 3 mg | ||
| magnesium stearate | MAGNESIUM STEARATE | 70097M6I30 | POWDER, FOR SUSPENSION / ORAL | 120 mg | ||
| glycerin | GLYCERIN | PDC6A3C0OX | ELIXIR / ORAL | 5621 mg | ||
| sodium hydroxide | SODIUM HYDROXIDE | 55X04QC32I | INJECTION / INTRATHECAL | 176 mg | ||
| sodium hydroxide | SODIUM HYDROXIDE | 55X04QC32I | SOLUTION/ DROPS / TOPICAL | ADJ PH | ||
| methylparaben | METHYLPARABEN | A2I8C7HI9T | EMULSION / TOPICAL | 0.2 %w/w | ||
| ascorbic acid | ASCORBIC ACID | PQ6CK8PD0R | SYRUP / ORAL | 200 mg | ||
| methylparaben | METHYLPARABEN | A2I8C7HI9T | AEROSOL, FOAM / TOPICAL | 0.16 %w/w | ||
| magnesium stearate | MAGNESIUM STEARATE | 70097M6I30 | TABLET / SUBLINGUAL | 17.5 mg | ||
| methylparaben | METHYLPARABEN | A2I8C7HI9T | SHAMPOO, SUSPENSION / TOPICAL | 0.15 %w/w | ||
| magnesium stearate | MAGNESIUM STEARATE | 70097M6I30 | LOZENGE / ORAL | 420 mg | ||
| sorbic acid | SORBIC ACID | X045WJ989B | SOLUTION / ORAL | 80 mg | ||
| glycerin | GLYCERIN | PDC6A3C0OX | INJECTION / SUBCUTANEOUS | 450 mg | ||
| sodium hydroxide | SODIUM HYDROXIDE | 55X04QC32I | INJECTION, EMULSION / INTRAVENOUS | ADJ PH | ||
| methylparaben | METHYLPARABEN | A2I8C7HI9T | SUSPENSION / AURICULAR (OTIC) | NA | ||
| glycerin | GLYCERIN | PDC6A3C0OX | TABLET, FILM COATED / ORAL | 1.55 mg | ||
| sodium hydroxide | SODIUM HYDROXIDE | 55X04QC32I | INJECTION / INTRASYNOVIAL | ADJ PH | ||
| sodium hydroxide | SODIUM HYDROXIDE | 55X04QC32I | SOLUTION / AURICULAR (OTIC) | 0.8 %w/w | ||
| methylparaben | METHYLPARABEN | A2I8C7HI9T | SOLUTION / RESPIRATORY (INHALATION) | 0.03 %w/w | ||
| glycerin | GLYCERIN | PDC6A3C0OX | INJECTION, SOLUTION / INTRAMUSCULAR | 15 %w/v | ||
| methylparaben | METHYLPARABEN | A2I8C7HI9T | DROPS / OPHTHALMIC | 0.01 %w/w | ||
| sodium hydroxide | SODIUM HYDROXIDE | 55X04QC32I | INJECTION / INTRACARDIAC | ADJ PH | ||
| magnesium stearate | MAGNESIUM STEARATE | 70097M6I30 | LOZENGE / TRANSMUCOSAL | 100 mg | ||
| ascorbic acid | ASCORBIC ACID | PQ6CK8PD0R | TABLET, FILM COATED / ORAL | 20 mg | ||
| sodium hydroxide | SODIUM HYDROXIDE | 55X04QC32I | SOLUTION / RESPIRATORY (INHALATION) | 8 %w/v | ||
| magnesium stearate | MAGNESIUM STEARATE | 70097M6I30 | TABLET, SUGAR COATED / ORAL | NA | ||
| sodium hydroxide | SODIUM HYDROXIDE | 55X04QC32I | INJECTABLE, LIPOSOMAL / INTRAVENOUS | ADJ PH | ||
| magnesium stearate | MAGNESIUM STEARATE | 70097M6I30 | IMPLANT / SUBCUTANEOUS | 0.5 mg | ||
| sodium hydroxide | SODIUM HYDROXIDE | 55X04QC32I | CREAM / VAGINAL | 0.19 %w/w | ||
| stearic acid | STEARIC ACID | 4ELV7Z65AP | SOAP / TOPICAL | 6 %w/w | ||
| sodium hydroxide | SODIUM HYDROXIDE | 55X04QC32I | SOLUTION / URETERAL | ADJ PH | ||
| methylparaben | METHYLPARABEN | A2I8C7HI9T | PASTE, DENTIFRICE / DENTAL | 0.05 %w/w | ||
| methylparaben | METHYLPARABEN | A2I8C7HI9T | SUSPENSION/ DROPS / OPHTHALMIC | 0.05 %w/w | ||
| sodium hydroxide | SODIUM HYDROXIDE | 55X04QC32I | SOLUTION / NASAL | 20 mg | ||
| sodium hydroxide | SODIUM HYDROXIDE | 55X04QC32I | POWDER, FOR SOLUTION / ORAL | ADJ PH | ||
| sodium hydroxide | SODIUM HYDROXIDE | 55X04QC32I | SOLUTION / INTRAOCULAR | ADJ PH | ||
| methylparaben | METHYLPARABEN | A2I8C7HI9T | SOLUTION / ORAL | 346 mg | ||
| sorbic acid | SORBIC ACID | X045WJ989B | TABLET, FILM COATED / ORAL | 5 mg | ||
| glycerin | GLYCERIN | PDC6A3C0OX | JELLY / VAGINAL | NA | ||
| sorbic acid | SORBIC ACID | X045WJ989B | TABLET, DELAYED RELEASE / ORAL | 0.03 mg | ||
| sodium hydroxide | SODIUM HYDROXIDE | 55X04QC32I | POWDER / INTRAVENOUS | ADJ PH | ||
| glycerin | GLYCERIN | PDC6A3C0OX | GUM, CHEWING / BUCCAL | 230 mg | ||
| sodium hydroxide | SODIUM HYDROXIDE | 55X04QC32I | INJECTION, SUSPENSION / INTRAVITREAL | ADJ PH | ||
| sodium hydroxide | SODIUM HYDROXIDE | 55X04QC32I | SOLUTION/ DROPS / OPHTHALMIC | ADJ PH | ||
| glycerin | GLYCERIN | PDC6A3C0OX | CAPSULE, EXTENDED RELEASE / ORAL | 265 mg | ||
| sodium hydroxide | SODIUM HYDROXIDE | 55X04QC32I | INJECTION, SOLUTION / INTRAMUSCULAR | 78 mg | ||
| glycerin | GLYCERIN | PDC6A3C0OX | GEL / TOPICAL | 500 mg | ||
| sodium hydroxide | SODIUM HYDROXIDE | 55X04QC32I | DISC / TOPICAL | ADJ PH | ||
| stearic acid | STEARIC ACID | 4ELV7Z65AP | TABLET, EXTENDED RELEASE / ORAL | 200 mg | ||
| magnesium stearate | MAGNESIUM STEARATE | 70097M6I30 | POWDER / ORAL | 25 mg | ||
| glycerin | GLYCERIN | PDC6A3C0OX | CREAM / VAGINAL | 60 mg |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 72a4fe26-76fb-4381-8bf3-b7c11cbe2229 | 2bf4bf54-b44b-489f-9f95-bb4bd270ba14 | 2010-09-04 | Warnings | 72a4fe26-76fb-4381-8bf3-b7c11cbe2229 2bf4bf54-b44b-489f-9f95-bb4bd270ba14 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
