Human Papilloma Virus (HPV)
- Manufacturer
- Newton Laboratories, Inc.
- Effective date
- 2020-12-10
- Label type
- HUMAN PRESCRIPTION DRUG LABEL
- Version
- 2
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 23:01:37
Label at a glance#
ProductHuman Papilloma Virus (HPV)
Active ingredientHUMAN PAPILLOMAVIRUS
Label structure10 sections
Contacts and useful links#
Label contents#
Full prescribing information#
INDICATIONS & USAGE SECTION
Law of similars - Use according to standard homeopathic indications
DOSAGE & ADMINISTRATION SECTION
Directions: Ages 12 and up, take 6 drops by mouth (ages 0 to 11, give 3 drops) as needed or as directed by a health professional.
ACTIVE INGREDIENT SECTION
Human Papilloma Virus 30c
PURPOSE SECTION
Law of similars - Use according to standard homeopathic indications
INACTIVE INGREDIENT SECTION
USP Purified water; USP Gluten-free, non-GMO, organic cane alcohol 20%.
QUESTIONS SECTION
newtonlabs.net - Questions? 800.448.7256
Newton Laboratories, Inc. FDA Est # 1051203 - Conyers, GA 30013
WARNINGS SECTION
WARNINGS: Keep out of reach of children. Do not use if tamper-evident seal is broken or missing. If symptoms worsen or persist for more than a few day, consult a doctor. If pregnant or breast-feeding, ask a doctor before use.
OTC - PREGNANCY OR BREAST FEEDING SECTION
If pregnant or breast-feeding, ask a doctor before use.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children.
PACKAGE LABEL
Products#
Every source-derived product name is available through these pages.
- Human Papilloma Virus (HPV)
- HUMAN PAPILLOMAVIRUS
- ALCOHOL
- WATER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 55714-6216 | 55714-6216-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| HUMAN PAPILLOMAVIRUS | 23CVL7WF4J | ACTIB |
| ALCOHOL | 3K9958V90M | IACT |
| WATER | 059QF0KO0R | IACT |
Source Document#
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 |
|---|---|---|---|---|---|---|
| 27e98841-7632-482b-e063-6394a90aef55 | 73016800-da38-d014-883d-544dd375ff4c | 2024-11-27 | Warnings | 73016800-da38-d014-883d-544dd375ff4c |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.