Herbal Power Alternative

Manufacturer
BELLS & MORE INC
Effective date
2021-03-16
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:39:01

Label at a glance#

ProductHerbal Power Alternative Amazing Powder Wound Antiseptic
Active ingredientZINC OXIDE
Label structure7 sections

Indications and uses

Dries oozing of poison ivy, oak, and temporarily relieves the pain and itch associated with: minor skin irritations, cuts, scrapes, burns insect bites, rashes, jock itch sunburn, diaper rash, chafing dermatitis decubital ulcers

Dosage and administration

Adults and children 2 years and older: apply freely up to 3 or 4 times daily. Under 2 years: ask a doctor before using. For best results, dry skin thoroughly before use.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Zinc oxide (12.5%)

Purpose

OTC - PURPOSE SECTION

Skin protectant

Uses

INDICATIONS & USAGE SECTION

Dries oozing of poison ivy, oak, and temporarily relieves the pain and itch associated with:

  • minor skin irritations, cuts, scrapes, burns
  • insect bites, rashes, jock itch
  • sunburn, diaper rash, chafing dermatitis
  • decubital ulcers

Warnings

WARNINGS SECTION

  • For external use only
  • Avoid contact with eyes. Not for genital area.

OTC - STOP USE SECTION

Stop use and ask a doctor if condition worsens or symptoms do not improve within 7 days or clear up and occur again within a few days

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of accidental ingestion, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Adults and children 2 years and older: apply freely up to 3 or 4 times daily.
  • Under 2 years: ask a doctor before using.
  • For best results, dry skin thoroughly before use.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Boric acid, Carbolic acid, Talc

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

57 g NDC: 81386-003-57

Zinc Oxide Powder 57 gZinc Oxide Powder 57 g

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2531381zinc oxide 12.5 % Topical PowderPSN2
2531381zinc oxide 0.125 MG/MG Topical PowderSCD2
2531381zinc oxide 12.5 % Topical PowderSY2
2531381ZNO 0.125 MG/MG Topical PowderSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81386-003-572022-07-29C16284748780-1e4f33bdf-a943-d8a0-e053-dadaa90a6e4eHPA Antiseptic Powder

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81386-003-57Herbal Power AlternativeAmazing Powder Wound Antiseptic57 g in 1 CONTAINERPOWDER572

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81386-003HERBAL POWER ALTERNATIVE AMAZING POWDER WOUND ANTISEPTIC (ZINC OXIDE) POWDER [BELLS & MORE INC]2Legacy NDC, 1 package rows20210317_bd99c49e-85b9-bc55-e053-2995a90a759d.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81386-00381386-003-57

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
PHENOL339NCG44TVIACT
TALC7SEV7J4R1UIACT
ZINC OXIDESOI2LOH54ZACTIB
BORIC ACIDR57ZHV85D4IACT

Source Document#

Source XML

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
bdaeabd5-e1b7-6bc1-e053-2995a90a89f5bd99c49e-85b9-bc55-e053-2995a90a759d2021-03-16WarningsExact identifier
spl id: bdaeabd5-e1b7-6bc1-e053-2995a90a89f5
spl set id: bd99c49e-85b9-bc55-e053-2995a90a759d

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.